Fri, 24 May 2013 04:06:24 UTCFri, 24 May 2013 04:06:24 UTCChemical Process Engineer
Lab Support is seeking a Chemical Process Engineer. Must have thermodynamic and mass transfer experience.
Responsibilities:
* Perform laboratory testing to define unit operations critical to process development and scale-up.
* Collect data, analyze, and interpret results to screen options and develop specifications.
* Work with the team to translate lab tests into a pilot production phase, then into a commercially viable industrial process.
* Operate the test/pilot equipment to manufacture finished product for characterization and additional testing.
* Develop and help maintain operating procedures and assist with operator training as necessary.
Required skills:

Requirements:
BS in Chemical Engineering (2-5 years of experience in process development and laboratory work)
* Demonstrate good problem solving and organizational skills.
* Experience with engineering drawings, equipment specifications
* Must have demonstrated outstanding communications skills working within a team environment
* Willingness to work "hands on" in the laboratory and production area's following all the facility safety guidelines
Contact:
Amy Ravelo at Amy.Ravelo@labsupport.com
Job Type:Employee
Job Status:Full Time
Locations:Multiple Locations
California-Marin County/North Bay
California-San Francisco
California-Silicon Valley/Peninsula

Categories:Multiple Categories
Biotechnology
Chemical Industry
Materials Science]]>Thu, 23 May 2013 10:28:59 UTCProduct Marketing Manager
Lab Support is seeking a passionate and motivated individual for the position of Product Marketing Manager for a leading biotech company based on the San Francisco Penninsula. The ideal candidate will participate in driving portfolio and technology directions by keeping a close pulse on the market, the compeitition, and the customers to provide feeback to the company to capture opportunities for growth. Bachelors degree in life sciences required, advanced degree and brand management experience preferred. Experience with reagents and next generation sequencing is mandatory.
Conducts market and competitor analysis within assigned product line(s)
Identifies unmet customer needs, develops new product definitions, manages product life cycle, and champions product portfolio strategies and product development priorities
Collaborates with Research and Development to translate user requirements to product specifications
through the identification and analysis of trade-offs and resulting implications
Actively participates on cross-functional project teams and drives smooth product launches
Works closely with a strategic partner to manage day to day operational issues
Works with stakeholders to develop and update marketing collateral
Anticipates and addresses needs of sales and distribution channels and geographies
Develops pricing and positioning ( including support data and/or analysis in collaboration with Finance )
Defines and implements marketing campaigns
Required skills:

Bachelors degree in life sciences or equivalent experience. Advanced degree a plus
2-3 years customer facing and/or marketing experience in a life sciences company required
Brand management experience preferred
Recent experience in genomics applications/tools industry required
Highly motivated and enjoy working both individually and as part of a team
Analytical with strong problem-solving skills and the ability to think creatively
Thorough and detail-oriented while keeping an eye on the big picture
Excellent communication, interpersonal and organizational skills
Flexible and adaptable and thrive in a fast-paced and rapidly-growing environment



Contact:
Amy Ravelo at Amy.ravelo@labsupport.com
Job Type:Employee
Job Status:Full Time
Locations:Multiple Locations
California-San Diego
California-San Francisco
California-Silicon Valley/Peninsula

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:59 UTCQC Lab Technician-Great Food Industry Opportunity!

·Conduct lab tests which include microbial
analyses, pH, moisture, ash, color, NIR,
and physical measurements
·Communicate with QA staff and production
management & line workers.
·Perform line checks throughout production
from incoming materials to finish product.
Verify accuracy of control devices and
measuring units. Perform visual
inspections of raw materials and finished
products.
· Collect samples for environmental
monitoring.
·Data collection related to HACCP and
regulatory guidelines.
·Communicate any production problems or
products that are out of specification.
·Troubleshoot any product defects.
·Maintain and organize retain samples
Required skills:


BS/BA Biology, Chemistry, Food Science, or related degree. Previous food industry or quality assurance experience is preferred, but not required. Must have excellent attendance, be detail-oriented, self-motivated, and work well independently. Excellent communication skills required and must have a basic understanding of science especially pertaining to food production and GMPs.


Benefits & Rewards:
* Competitive Salary
*Complete benefits including medical with premium reduction after 8 weeks, dental, short-term disability, life insurance, 401(k) plan
*Paid Holidays
*Appreciation bonuses and More!!


To Apply:
Email resume, apply online, or call
omaha@labsupport.com
www.labsupport.com
PH: 800.998.3332

Contact:
Anne Nelson
Job Type:Contract Hire
Job Status:Full Time
Locations:Multiple Locations
NE Nebraska
Nebraska-Omaha

Categories:Multiple Categories
Biotechnology
Food & Beverage]]>Thu, 23 May 2013 10:28:59 UTCQA Lab Technician
Work Responsibilities:
- Work in field of virus production of animal health pharmaceuticals
- -Assist in coordination and manufacture of high quality products in a manner that is efficient, cost-effective and compliant that meet the business plan.
- Review and prepare documents and changes i.e., PO, SO, SOP’s
- Participate in multifunction teams
- Produce departmental reports and analyze data
- Organize and schedule work flow for associates
- Adapt well to change and participate in changing environment, i.e. conduct experiments, evaluate equipment, suggest capital
- May act as a lead person in supervisor’s absence.
- Comply with all company standards, i.e., HSE, USDA
Required skills:

Qualifications:
BS degree preferred or equivalent combination of education and experience. Previous experience in relevant field required.

Benefits & Rewards:
Competitive compensation, bonuses, and benefits including medical, dental, life, 401(k) and paid holidays.
Contact:
Anne Nelson Anne.nelson@labsupport.com www.labsupport.com 515.440.6447 (toll-free 800.998.3332)
Job Type:Employee
Job Status:Full Time
Locations:Multiple Locations
Larchwood, IA
Iowa-Western/Sioux City

Categories:Pharmaceutical]]>Thu, 23 May 2013 10:28:59 UTCSr. Coatings Chemist
GENERAL SUMMARY:
The role of this position is crucial in the development of new products and the reformulation of current products; perform testing to verify the products meet product specifications as set in conjunction with the sales and marketing functions. The Sr. Coatings Chemist will assist in supporting the Director of Global Technology and sales and marketing teams with interactions across functional groups to develop automotive refinish coatings. This position also will develop and support the global technical requirements for Pro-Spray Automotive Finishes to meet internal and external needs in the product line.
The Sr. Coatings Chemist will be required to supervise a Lab Technician/Jr. Development Chemist(s).

ESSENTIAL JOB FUNCTIONS:
SAFETY & LEGISLATION
1. Actively participate in safety meetings and requirements to meet safety standards within the working environment. ( manage self & teams safety targets)
2. Be aware of changes in legislation such as VOC, HAPS heavy metal restrictions, etc. as they pertain to product development, as well as any REACH or similar programs for regions that we sell into and need to meet these requirements for raw materials, labeling, shipping, etc.
PEOPLE DEVELOPMENT
1. Plans, organizes and performs experiments relating to paint development. Manages resources (people and equipment) to meet project priorities and targets.
PRODUCT DEVELOPMENT
1. New Product development of following types of paint coatings: Clear coats, Basecoats, Primers, Activators and Reducers for automotive refinish.
2. Reformulation of current coatings to meet changing market needs either as a response to legislation, testing criteria or customer specific needs or problems.
3. Knowledge of most of the following Chemistry Types: Epoxy/amine cured, isocyanate/polyol (polyurethane) 2K systems. Acrylic, polyester, latex based paints, waterbased and solvent based coatings.
4. Perform all types of physical tests and investigations in connection with development and reformulation of automotive aftermarket refinish products, such as hardness, weathering, solvent resistance, corrosion gloss, DOI and humidity.
5. Provides support to Production, QC and technical service groups, as well as help for customers service questions from a technical aspect.
6. Develop solid color and special effect tinters to meet the ever expanding range of automotive colors on the market.
COST CONTROL:
1. Work with supplies to find ways to identify and evaluate raw materials in an effort to keep costs low, reduce complexity, improve performance or meet regulatory requirements, as well as supplier shortages or forced material changes.
2. Work with manufacturing, QC and Technical Service to ensure consistent high quality products.

Required skills:

KNOWLEDGE/SKILLS/ABILITIES:
Have a basic grasp of the vehicle repair industry from the coatings side of the business, (vehicle paint repair, adhesion sanding, color match)
Understand the basic chemistries involved for automotive product development, resin types, pigments, additives and solvents in urethane, Isocynates and Epoxy systems. Beneficial to have worked on solvent and water based systems.
Good understanding of color matching/color theory (spectro DE CMC).
Capable of completing competitive testing, benchmarking studies and report findings.
Beneficial to be flexible, creative, have initiative and have the ability to carry out laboratory based experiments with the required precision to work collaboratively.
Strong communication skills (must be able to explain results verbally and in written form)
Keep detailed records of experiments, testing and results
Set up suitable QC methods on new products.

EDUCATION/EXPERIENCE:
1. Bachelor Degree in Science, majoring in Chemistry or similar field, equivalent experience would be considered.
2. Eight to ten years work experience within the automotive aftermarket coating industry, preferred.
3. Working knowledge of the chemistries involving: 2pack crosslinking resins, epoxies, polyesters, hydroxyl acrylics and latex with isocyanates and amines.

Contact:
Anthony Capezzuto
Job Type:Employee
Job Status:Full Time
Locations:Multiple Locations
Ohio-Akron
Ohio-Cleveland

Categories:Chemical Industry]]>Thu, 23 May 2013 10:28:58 UTCQA Manager
Primary Function
Manage the EA ISO Quality Assurance Program to ensure compliance to the standard as well as internal policies and procedures.
Develop and control the EA integrated Management System (QA, Environmental and Safety) for all sites.
Lead the Internal Audit Program, the internal Corrective/Preventive Action and Management Review programs.
Drive the Continuous Improvement Program for Painesville/Louisville/Schererville. Work across departments to initiate programs that increase productivity and /or reduce waste
Major Job Functions
Ensure compliance to ISO 9000 standard including ISO mandated updates/changes for ECKART America.
Implement & Maintain an EA Integrated Management System (ISO 9000, 14000 & 18000) for the entire EA organization. Document distribution and control to be done through new software.
Manage the Quality Assurance and the Environmental Internal Audit Program including training of auditors, scheduling of audits & overseeing reporting.
Lead the ISO 9000 training program.
In coordination with management, develop and maintain a continual improvement and quality tracking system.
Coordinate the preventive action portion of the Customer Complaint system and manage the ECKART Initiatives system to ensure timely and complete responses to internal and external customers as well as monitor success of corrective actions.
Manage and lead Continuous Improvement projects for EA. Must be able to work closely with Operations Team, Process Engineering, and Capital Project Manager.
Must document improvement projects and track status and results. Constantly look for opportunities to improve processes, increase productivity, and reduce scrap and waste.
Lead Management Review meetings.
Respond to customer quality audits.
Participate in environmental issues as needed.



Required skills:

Position Requirements
BS in Science or Engineering Field
Internal Auditor Certification
Quality Assurance Training / Certification
5 Years Minimum in a Quality Assurance Management position combined with Process Improvement Experience-(Six Sigma Black Belt and /or Lean Manufacturing)
Requires 50% travel
Compensation 75,000 with 10% bonus
Contact:
Anthony Capezzuto
Job Type:Employee
Job Status:Full Time
Locations:Multiple Locations
Ohio-Painsville
Ohio-Columbus/Zanesville

Categories:Materials Science]]>Thu, 23 May 2013 10:28:58 UTCLaboratory Technician for a Great Company!
We are seeking Lab Technicians for a 1 year contract opportunity with leading manufacturer located in the near west side of Cleveland.


Responsibilities include:

Will be working in a laboratory environment preparing paint and spraying panels for testing purposes.
Will be working with equipment and ovens to complete the customer orders.

Shifts Available:
5:00 a.m. to 5:30 p.m. (FRI SAT SUN or SAT SUN MON)
5:00 p.m. to 5:30 a.m. (FRI SAT SUN or SAT SUN MON)

Compensation is 12.55/hr
Required skills:

Requirements include:
Laboratory experience or Auto body shop experience.
Must be able to stand for up to 12 hours per day.
Strong attention to detail
Experience working in an industrial or paint lab is a plus .
Contact:
Anthony Capezzuto
Job Type:Employee
Job Status:Full Time
Locations:Ohio-Cleveland

Categories:Chemical Industry]]>Thu, 23 May 2013 10:28:58 UTCManufacturing Manager/Engineering Manager
The Manager/Director of Engineering is responsible for leadership of the Engineering team in support of the company’s goals for capacity expansion, cost reduction, quality improvement, and product/process introduction, safety, and on time delivery.
Responsibilities
•Build, guide, and motivate a strong technical team.
•Develop and monitor performance to an engineering budget that supports the company’s goals.
•Utilize technical and business knowledge, experience, and leadership skills to identify, understand, and act on the key opportunities for improvements in process and product cost and quality.
•Provide technical and project management leadership for aggressive capacity scaling initiatives including technology selection and evaluation, supplier selection, risk assessment, process design, facility design, budget management, process qualification, and ramp to metrics.
•Provide technical guidance and support to other departments as needed in the areas of equipment selection, risk assessment, facility implication, etc.
•Utilize Lean and 6 Sigma tools and methodologies in the process control, problem solving, and continuous improvement of our processes and products.

Required skills:

•10+ years of experience in chemical or materials manufacturing
•5+ years of Engineering Management experience. Operations management experience is a plus.
•B.S/ B.A in Chemical or Mechanical Engineering Required; Masters in Engineering Preferred
•Possess a broad understanding of multiple engineering disciplines.
•Experience leading technical capital projects for the establishment of new manufacturing sites or production lines.
•Solid understanding of and experience successfully executing Lean and 6 Sigma tools and methodologies
•Effective communication skills, both verbally and in writing, with superiors, colleagues and individuals insides and outside of the company.
•Strong initiative and desire to work in a team environment.
•Strong organizational, people and communication skills.
•Thrives in an entrepreneurial environment
Contact:
Baltimore Lab Support
Job Type:Contract Hire
Job Status:Full Time
Locations:Maryland-Baltimore

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:58 UTCQuality Assurance Scientist
SUMMARY:
The Quality Assurance Scientist will lead the development, coordination, implementation, and maintenance of the Safe Quality Food (SQF) Code certification program for the facility.
The QA Scientist will create and maintain corporate level quality policies which align with the SQF code and support the plant in improving current programs and implementing new programs tailored to the needs of the individual manufacturing facility.
The QA Scientist will be expected to make recommendations and decisions which positively impact the Quality System and the organization.
Additionally, this position is also responsible for managing the following programs: document management, internal auditing, verification validation, supplier approval, and corrective action.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Coordinate development, implementation, and maintenance of SQF at the facility
Support development, implementation, and maintenance of SQF at the other manufacturing and packaging facilities
Represent the manufacturing facility as the Designated SQF Practitioner
Manage Corporate Quality documentation
Manage and ensure compliance to verification and validation schedules
Manage and ensure compliance to the Internal Audit Program
Manage and ensure compliance to the Supplier Approval Program
Lead supplier and contract manufacturer audits as needed
Manage follow-up on corrective actions for the facility
Some travel between manufacturing facilities
Other duties and projects as assigned by the QA Director

Required skills:

QUALIFICATIONS:

Education: Bachelor of Science degree in Food Science, Microbiology, Chemistry, Biology or related discipline required.

Experience:
5 - 8 years or previous quality assurance experience in a food manufacturing facility required.
SPC, SQF, BRC, ISO 22000, or ISO 9001 experience strongly preferred.

Skills:
Excellent communication skills, verbal and written
Ability to communicate with all levels of the organization
MS Word
MS Excel
MS Access (preferred)
Contact:
Call us NOW if you are interested in learning more about this exciting opportunity! 763-546-0512
Job Type:Employee
Job Status:Full Time
Locations:Minnesota-Minneapolis

Categories:Food & Beverage]]>Thu, 23 May 2013 10:28:58 UTCMicrobiology Technician
The Laboratory Technician will be capable of effectively performing all microbiological methods used in the Micro Lab, recording results, reviewing and interpreting data, preparing and distributing reports. The Laboratory Technician will have responsibility for the ongoing operations of the Micro Lab, including laboratory and equipment maintenance, and adherence to applicable regulations and GLP’s. The Laboratory Technician will manage the Liquid and Dry Egg Vendor Audits, egg vendor/product approvals and collaborative testing; maintain Micro COA verification, Micro Action Notice, and Environmental Micro Sampling programs.

Main Job Responsibilities/Activities:

1. Receive and prepare samples for analysis. Record sample information in lab notebook and assign sample numbers. Mark plant sample charts and review COAs.
2. Practice good aseptic technique to prepare lab samples. Perform all microbiological analyses according to the current approved methods used in the Micro Lab. Store retainer samples appropriately.
3. Maintain accurate lab notebooks and files. Document all analyses performed and the results. Record data in the Micro Lab database. Prepare and distribute reports to required personnel. Send Micro Action Notices, holds, and releases to plant QA managers.
4. Prepare media and reagents for use in the lab. Perform maintenance checks on equipment. Clean glassware and utensils. Monitor inventories of lab supplies and purchase as needed.
5. Manage the Micro Sampling and COA Verification program. Develop familiarity and understanding of microbial specifications for ingredients and products. Note unusual results and trends. Assist with the determination of causes and solutions for out of specification results or adverse trends. Follow-up on COA deficiencies.
6. Administer the Liquid and Dried Egg Vendor Auditing Programs. Contact vendors for audit samples, monitor receipt, perform analyses, release products, and send reports.
7. Coordinate approval of new egg vendors or SKUs. Perform collaborative testing, monitor results. Work with the vendor, Purchasing, R&D, and Analytical personnel to complete approval process. Assess results and provide recommendations.
8. Manage environmental sampling programs. Assist plants with analyses of results troubleshooting, and corrective action plans.
9. Maintain Micro Lab GLP program. Conduct Micro Lab environmental testing, autoclave sterilization checks, media control documentation. Develop technical standards for all methods and procedures used in the Micro Lab. Update existing technical standards as needed.
10. Maintain an orderly and safe lab environment. Be aware of and adhere to the Chemical Hygiene plan and lab safety procedures and requirements. Report all accidents or issues to the Corporate Microbiologist or Chemical Analyst.
11. Provide assistance and training for Lab Assistant. Assume additional responsibilities and work on special projects as assigned. Adhere to mission of Company and to the Company Code of Ethics.
Required skills:

Bachelor’s Degree (BA or BS) in Microbiology, Food Science or Biology with some practical experience in a food microbiology lab required. Strong communication, critical thinking and decision-making skills. Ability to prioritize and organize time and materials, with excellent attention to details. Able to work independently and as part of a team.

Preferred Background/Experience:

Bachelor’s Degree in Microbiology, Food Science or Biology with at least 2 years practical experience in a food microbiology lab preferred. Food plant experience a plus.
Contact:
Call us now to find out more about this exciting opportunity! 763-546-0512 Minneapolis@LabSupport.com
Job Type:Employee
Job Status:Full Time
Locations:Minnesota-Minneapolis

Categories:Food & Beverage]]>Thu, 23 May 2013 10:28:58 UTCChemist
We have an exciting contract opportunity for a Chemist with a great pharmaceutical client in northern Rhode Island!

Responsibilities:

Performing and documenting QC in-process testing, release testing and stability analysis of manufactured products as per SOPs,
Performing wet chemistry methods per compendia methods or in house SOPs
Provide timely and complete data, data review, and reporting of OOS or OOT results.
Principal duties include performing HPLC analysis (RP), Gas Chromatography, spectrophotometric analysis, various analytical chemistry techniques, analysis, all per USP methods and/or qualified QC SOPs.
Assist with overall maintenance of QC laboratory, including maintaining Agilent HPLC systems, handling and tracking of samples, and data management.
Drafting and reviewing SOPs and documentation to support ongoing activities in the QC department.
Assist in optimization of QC testing methods, which may include supporting analytical method transfer and method validation activities.
Perform troubleshooting analysis on equipment and assays. Assist in maintaining and cleaning the laboratory and applicable equipment.

Required skills:

BS or equivalent in Chemistry or related scientific discipline
0-2 year's cGMP Quality Control laboratory experience including HPLC methods, documentation, data analysis, and data trending.
Experience with a variety of analytical techniques, with hands-on sample preparation and HPLC experience being most important.
Experience with data analysis including HPLC software systems, trending analysis (MS Excel), and proficiency with MS Word is required.

Contact:
Chelsea Gerard
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:Rhode Island-Providence

Categories:Pharmaceutical]]>Thu, 23 May 2013 10:28:58 UTCLab Technician
Lab Support has an immediate need for a Lab Technician.
This is a contract to hire position.
Company: Chemical Company
Location: South Chicago

Days/Shift: Monday thru Friday (must be flexible to work weekends) Second shift (2pm-10:30pm)

Job Description: The Laboratory Technician will perform instrumental and wet chemistry analysis on raw and acidulated soap stock, vegetable oils, and inedible grease adhering to AOCS methodology.


Responsibilities: · Operate Near Infra-Red
· Perform routine sample analysis of raw and acidulated soap stock (TFA,FFA, Unsap, IV, Moisture)
· Data entry of laboratory samples and analytical data
· Maintain organization of sample retains
· Perform routine boiler water analysis (alkalinity, sulfite, chloride, pH, Conductivity)
· Operate Near Infra-red and Auto titration equipment
· Prepare samples for GC and GC\MS analysis
· Perform analytical testing on new sources of raw materials
· General laboratory housekeeping
· Familiar with Microsoft Office Applications




Required skills:

Qualifications: Education: BA/BS Biological Sciences or Chemistry

Experience: 6 mos.-2 years experience working in a laboratory environment
Contact:
chicago@labsupport.com
Job Type:Contract Hire
Job Status:Full Time
Locations:Illinois-Chicago South

Categories:Chemical Industry]]>Thu, 23 May 2013 10:28:58 UTCSr. R&D Chemist


Lab Support has an immediate direct hire opportunity for a Senior-level Formulation Chemist.

Company: Personal Care

Location: South suburbs

Days/Shift: Monday thru Friday first shift

Job Description:

Essential Functions:
New Product Development
Develop new formulations and product applications for the ethnic category that are in compliance with domestic and international regulations
Research and identify new and innovative technologies
Critically analyze unexpected issues in formulations and implement solutions
Monitor stability and validate formulations through efficacy testing, toxicological/microbiological testing, and other necessary tests
Implement and monitor cost parameters in formulations
Prepare relevant documentation to formulations including MSDSs, manufacturing processes, etc.
Assist in piloting and scale-up efforts of new formulations
Maintain awareness of competitive products, applications, technical developments in related fields of science and market trends as they relate to ethnic care and other similar categories
Assist in regulatory compliance matters
Keep current on changes in regulatory and how they affect current and future projects
Create documentation for regulatory compliance
Maintain and enforce laboratory SOPs, manage laboratory compliance and systems
Identify gaps in laboratory and product development processes and recommend solutions
Communicate development challenges to management on a timely basis, while offering alternative solutions
Manage multiple projects and meet expected deadlines and goals
Mentor, teach and share expertise with junior staff to help develop talent
Required skills:

Minimum Education and Experience:
Advanced degree in Chemistry, Chemical Engineering or other relevant scientific field preferred. At least 5+ years of experience in industry, with an emphasis on lab bench formulation in hair products. Experience in the ethnic industry a plus.
Knowledgeable in FDA, cGMP, and OSHA regulations and other international cosmetic regulations
Experience writing/revising SOPs and claims substantiation
Highly proficient in the use of personal computers and experienced with Microsoft Office Suite
Understanding of int’l cosmetic regulations (i.e. EU Directive, Health Canada, African regions, etc.)
Contact:
chicago@labsupport.com
Job Type:Direct Hire
Job Status:Full Time
Locations:Illinois-Chicago South

Categories:Multiple Categories
Chemical Industry
Personal Care]]>Thu, 23 May 2013 10:28:58 UTCSenior Microbiologist
Lab Support has an immediate need for a Senior Microbiologist.

This is a contract to hire position.

Company: Food Industry

Location: South suburbs

Days/Shift: Monday thru Friday first shift

Job Description:
Ideal candidate will have experience working as a Microbiologist in the Food Industry
Plan, lead, and execute varieties of projects from inception to completion
Duties include: over site of personnel, must be proficient in technical writing
Microbiology techniques include: streaking plates, inoculation, proficiency testing etc...
Looking for a leader to guide a team!
Compensation: $60-$75k/year

Required skills:

MS in Microbiology or other related field with 3-5 years experience
BS in Microbiology or other related field with 7-10 years experience

ONLY LOCAL CANDIDATES WILL BE CONSIDERED
Contact:
chicago@labsupport.com
Job Type:Contract Hire
Job Status:Full Time
Locations:Illinois-Chicago South

Categories:Food & Beverage]]>Thu, 23 May 2013 10:28:48 UTCCompliance Manager

Essential Duties
· Provide leadership, direction and guidance to plant personnel by understanding regulatory, customer and internal quality/food safety requirements.
· Provide solution or prevention of problems compromising regulatory compliance throughout entire business segment that includes investigation of issues, corrective action and recommendations of issue resolution.
· Coordinates area work flow for QA Technicians concerning regulatory activities.
· Provides plant-wide employee training on regulatory compliance.
· Leads the development of training materials and formats that training to ensure its effectiveness.
· Instrumental in developing, initiating, maintaining and revising policies and procedures for the general operation of the Compliance Program and its related activities.
· Maintains up to date regulatory awareness and understanding in field; makes recommendations to plant management to assure compliance.
· Undertakes assignments of high complexity to support the Director of Quality.
· Supports the Global Food Safety Initiative (GFSI) efforts within the plant. Interacts with regulatory officials on behalf of the plant by leading regulatory inspections.
· Verifies and validates changes to the Food Safety and Food Quality Plan.
· Maintain close team working relationship with all operations group leader/supervisors and maintenance supervisors.
· Provides support and /or participates in 3rd party and internal audits.
· Other Duties as assigned.


International Nutraceutical Company is seeking a Compliance Manager to join their team!
Required skills:

· B.S in Food Science, Microbiology or related field requirements, Masters Preferred
· Safe Quality Food (SQF) Practitioner certification proffered
· Strong Knowledge of federal and state food industry regulations (i.e. FDA, USDA, etc)
· Proven track record of leading compliance teams preferred
· Minimum 5 years compliance and regulatory; experience working in manufacturing plant required
· Must possess expert knowledge of 21 CFR PART 110, 111, 113, and 114.
· Strong knowledge of GFSI standards.
· Strong knowledge of plant QA systems (i.e. HACCP, sanitation and pest control practices, etc)

Contact:
Chris Quevedo
Job Type:Employee
Job Status:Full Time
Locations:Multiple Locations
California-Los Angeles
California-Orange County

Categories:Multiple Categories
Food & Beverage
Pharmaceutical]]>Thu, 23 May 2013 10:28:48 UTCAssociate Scientist
Non-regulated pharmacokinetic (PK) study sample management. Includes sample tracking, receipt, storage, organization and preparation for analysis, reshipping and final disposition. The individual will also contribute to the analysis of Biotherapeutic PK samples using ligand binding assays (LBA) using a range of platforms (ELISA, ECL, Gyros, etc) working closely with lead bioanalytical scientists in the Ligand Binding Assay Group.
Responsibilities:
Responsible for non-regulated study sample management. Responsible for replenishing lab supplies, preparing buffers and reagents, helping to setup studies (i.e. organizing and labeling tubes etc) and helping to ship out items when needed. Responsible for assisting with discovery PK assay life cycle support (reagents and buffers for assay and instrument platform). Prepare of samples for analysis which may include automation. Depending on ability may also independently conduct sample analysis by ELISA and related methods.
Position Details

THIS IS A PROJECT-BASED ASSIGNMENT AND FORECASTED TO RUN AT LEAST TWO YEARS
Full time (40/Week)

No Travel Required

Required skills:

Qualifications:
3+ years industry experience ideally with a focus in on PK LBA analysis of Biotherapeutics or experience in a medical technology/laboratory medicine setting focusing on sample analysis. Working knowledge of immunoassays. Excellent attention to detail
Willingness to learn with a strong work ethic.
Technical Skill Requirements:
Proven ability to generate high quality data. Strong organizational and time management skills in order to balance working on multiple projects in parallel. Understanding and skills in bioanalytical laboratory techniques. Experience with project management beneficial. Experience with laboratory information management systems beneficial. Knowledge of PK beneficial

This position will focus on non-regulated pharmacokinetic (PK) study sample analysis using ligand binding assays. Intermediate candidate with ideally CRO or Pharma PK bioanalytical experience.

MOST CRITICAL: Experience with quantitative ligand binding assays (ELISA ) and sample processing. Sample management and logistics.
REQUIRED PERSONALITY TRAITS: Highly organized and quality conscious, good communication skills, willingness to learn, customer focus. Ability to execute reliably.
Skills Required 4-7 Years:
Analytical Techniques
Immunoassays (RIA, ELISA)
Sample Analysis

Contact:
connecticut@labsupport.com 203 272-9998
Job Type:Employee
Job Status:Full Time
Locations:Multiple Locations
Connecticut - Groton
Connecticut-Hartford
Connecticut-New Haven
Rhode Island-Providence

Categories:Pharmaceutical]]>Thu, 23 May 2013 10:28:48 UTCAssociate Scientist
Non-regulated pharmacokinetic (PK) study sample management. Includes sample tracking, receipt, storage, organization and preparation for analysis, reshipping and final disposition. The individual will also contribute to the analysis of Biotherapeutic PK samples using ligand binding assays (LBA) using a range of platforms (ELISA, ECL, Gyros, etc) working closely with lead bioanalytical scientists in the Ligand Binding Assay Group.
Responsibilities:
Responsible for non-regulated study sample management. Responsible for replenishing lab supplies, preparing buffers and reagents, helping to setup studies (i.e. organizing and labeling tubes etc) and helping to ship out items when needed. Responsible for assisting with discovery PK assay life cycle support (reagents and buffers for assay and instrument platform). Prepare of samples for analysis which may include automation. Depending on ability may also independently conduct sample analysis by ELISA and related methods.
Position Details

THIS IS A PROJECT-BASED ASSIGNMENT AND FORECASTED TO RUN AT LEAST TWO YEARS
Full time (40/Week)

No Travel Required

Required skills:

Qualifications:
1-3 years industry experience ideally with a focus in on PK LBA analysis of Biotherapeutics or experience in a medical technology/laboratory medicine setting focusing on sample analysis. Working knowledge of immunoassays. Excellent attention to detail
Willingness to learn with a strong work ethic.
Technical Skill Requirements:
Understanding and skills in bioanalytical laboratory techniques. Proficient in the use of standard laboratory equipment and preparation of buffers and reagents. Proven ability to generate high quality data. Strong organizational and time management skills in order to balance working on multiple projects in parallel. Experience with laboratory information management systems beneficial.
This position will focus on non-regulated pharmacokinetic (PK) study sample management; seeking Base/Entry candidate. However, will consider Intermediate candidates with bioanalytical experience.
MOST CRITICAL: Experience with quantitative ligand binding assays (ELISA ) and sample processing. Sample management and logistics.
REQUIRED PERSONALITY TRAITS: Highly organized and quality conscious, good communication skills, willingness to learn, customer focus. Ability to execute reliably.
Skills Required 1-3 Years:
Analytical Techniques
Immunoassays (RIA, ELISA)
Sample Analysis

Contact:
connecticut@labsupport.com 203 272-9998
Job Type:Employee
Job Status:Full Time
Locations:Multiple Locations
Connecticut - Groton
Connecticut-Hartford
Connecticut-New Haven
Rhode Island-Providence

Categories:Pharmaceutical]]>Thu, 23 May 2013 10:28:48 UTCQuality Assurance & Food Safety Manager
The QA Food Safety Manager will:
Ensure compliance with all regulatory requirements
Monitor production facilities for compliance with all safety, quality and reliability standards
Implement and monitor compliance with corporate policies
Develop and implement department business plans (short - mid term) and assist in long-term strategic plant plans
Make recommendations regarding manufacturing methods and sanitation practices to management.
The QA Food Safety Manager will manage a staff of 4-8 QA personnel. This position will be responsible for quality and food safety programs including: microbiological testing, quality control testing and maintenance of the weight and defect control programs.
The QA Food Safety Manager will develop operating procedures and ensure plant personnel's understanding and compliance with policies. This position will be responsible for training, mentoring and ensuring the morale of personnel to optimize their performance and promote career growth.
Perform performance reviews and counsel performance problems.
Investigate and resolve complaints about plant products, maintaining necessary records regarding the problem's resolution.
Meets with vendors, customers and quality representatives and other company staff to discuss and resolve quality issues.
Monitor and ensures that the company's product "hold" policies and procedures are communicated to plant staff and that the plant adheres to the procedures. As appropriate, will order the suspension of production or the release of product when food safety and/or quality standards are not achieved.
Leads quality audits of the plant.
Participates in regular meetings with plant management to discuss quality improvements.
Ensures that all GMP and Safety standards are in compliance. Participates in scheduled GMP, sanitation and safety inspections throughout the production departments and corrects, or issues work orders to correct, any identified deficiencies.
Follows up on work orders, with the appropriate Associates to ensure expeditious performance of the requested work.
Keeps abreast of latest food safety, quality and manufacturing technologies, systems, and practices.
Maintains a comprehensive understanding of all products manufactured by the plant as well as the raw materials, packaging materials, and operations required in the manufacturing process including quality specifications and standards.

Required skills:

Bachelors degree in (Food Science, Engineering or related field)
Minimum 5 years experience is required with at least 2 years of supervisory experience in a food-processing, or pharmaceutical organization, preferably using computerized manufacturing equipment.

o Good team building skills
Demonstrated knowledge and application of statistical process control, quality assurance techniques and tools and quality management principles in a food or pharmaceutical manufacturing environment.
Working knowledge of FDA regulations, Good Manufacturing Practices (GMPs), HACCP, food allergens, pest control, and food microbiology.
Demonstrated knowledge of efficient and safe manufacturing operations to include product and associate safety, OSHA standards, product quality (success rates), and cost control (minimizing downtime and waste, optimizing yield).
Demonstrated ability to direct, coach, and train associates as well as plan, monitor and schedule work.
Demonstrated ability to formulate and understand mathematical equations, especially basic statistical analysis.
Strong PC proficiency to include Microsoft Office Word, Excel, PowerPoint; Working knowledge of statistical software programs.
Contact:
connecticut@labsupport.com 203 272-9998
Job Type:Employee
Job Status:Full Time
Locations:Multiple Locations
Connecticut-Hartford
Connecticut-New Haven

Categories:Multiple Categories
Food & Beverage
Food & Beverage]]>Thu, 23 May 2013 10:28:48 UTCLead Chemist

Growing Nutraceutical and Vitamin Supplement Manufacturer is seeking a Lead Chemist to join their team.

Summary
The Chemist is responsible for providing support to Lab Departments, to ensure that all testing is performed in accordance with company written Standard Operation Procedures (SOP), Analytical Procedures, and/or USP/NF Compendia.

Duties and Responsibilities
• Performing wet chemistry, HPLC, GC, Dissolution test, UV, PH.
• Performing analytical tests of raw material, in-process, and finished products.
• Calibrating instruments used for QC testing.
• Documenting test results, problems and other issues, performing initial troubleshooting issues that arise during analysis, conducting all analysis and documentation using GMP and FDA guidelines.
• Investigating OOS issues and implementing corrective actions.
• Performing laboratory instrument validations (IQ, OQ, PQ).
• Performing method validations.
• Performing cleaning validations.
• Other duties, assignments and tasks as assigned by VP or senior management.

Required skills:

• BS Degree in Chemistry (minor in Microbiology) in an accredited college/university; plus
• Five (5) or more years of work experience performing analytical chemistry in a regulated industry (i.e. Pharmaceutical, Medical Device, Biopharmaceutical, and/or Nutraceutical) and work experience conducting validation (instrument, method, cleaning and process).
• Knowledge and understanding of quality in a manufacturing environment, as well as laboratory controls and work safety rules/regulations.
• Ability to present information in one-on one and small group situations with customers, management, and other employees of the organization.
• Willing to work late and/or during weekends; if needed.

Contact:
Costa Mesa Lab Support
Job Type:Employee
Job Status:Full Time
Locations:California-Los Angeles

Categories:Multiple Categories
Nutraceutical & Vitamin Supplement
Pharmaceutical]]>Thu, 23 May 2013 10:28:48 UTCQuality Manager
Growing In-vitro Diagnostic Medical Device Company is seeking a Quality Manager to join their team.

The ideal candidate will have over 5 years of Quality Assurance & Quality Systems Managerial experience in the IVD industry. Must have knowledge and prior application experience with QSR, ISO 9001, and ISO 13485. ASQ CQA or CQLA certification is highly desired. The company offers competitive pay, full benefits, a cohesive work atmosphere, alternative work schedule, and a dynamic work environment.

Duties and Responsibilities
• Manage and oversee component release for packaging based on analytical results.
• Supervise reagent raw material release into inventory.
• Ensure company-wide compliance with state, federal and international regulations and standards, as appropriate.
• Manage and oversee:
o The data collection and analysis system
o The document control system
o The administration of the corrective and preventive action system
o The raw materials testing function
• Communicate, both orally and in writing, with customers and suppliers, as appropriate.
• Coordinate the regular Issues Investigation meeting and follow up on action
• Participate in the company Management Review as appropriate.
• Supervise all aspects of the quality testing function for all diagnostic and control products.
• Coordinate with other departments in examining operational or functional problems that affect product quality.
• Assist with preparation of work instructions and specifications, as appropriate.
• Resolve all non-conformances.
• Contribute to the testing program for customer complaints.
• Participate in the development of new products, as appropriate.
• Review Engineering Change Documents, as appropriate.
• Ensure department equipment is properly maintained and calibrated.
• Prepare and communicate performance reviews for all laboratory personnel.
• Monitor Quality department labor and cost variances.
• Prepare the annual budget for the Quality Laboratory cost center.
• Assist in conducting failure investigations, corrective action and preventive action, as appropriate.
• Ensure department personnel are adequately trained in the performance of their jobs.


Required skills:

• B.S. in Chemistry, Biology, Biotechnology, Molecular Biology or related
• Has 5 – 10 years’ quality systems experience (QA, QC, Compliance)
• Has 2+ years supervisory Managerial/Leadership experience
• Has experience in the medical device manufacturing field
• Has working and applied knowledge of the FDA QSR (Quality System Regulation), ISO9001, ISO13485 and standard laboratory practices
• Has experience with an internal audit system Quality System Audits
• Understands the importance of focus on safety, compliance, operational excellence and financial performance.
• Demonstrates professional leadership with the proven ability to build business relationships
• Has proven influence, leadership and facilitation skills.
• Proactively identifies issues and seeks resolution within the team.
• Demonstrates organizational skills, and is capable of managing multiple tasks.
• Has the ability to pay attention to details and accuracy while being flexible and able to adapt to changing priorities
• Thrives in a fast-paced environment
• Is able to manage time with respect to priorities
• Can communicate effectively across all levels of the organization.
• Has direct experience interfacing with the FDA and ISO auditors
• Has experience in in vitro diagnostics medical device
• Has experience with Canadian medical device regulations and European in vitro diagnostic directives
• Has a Certification issued by the American Society for Quality
• Is a Certified Quality Auditor or Certified Quality Lead Auditor
• Has direct experience with validations (process, equipment, software)

Contact:
Costa Mesa Lab Support
Job Type:Employee
Job Status:Full Time
Locations:California-Orange County

Categories:Multiple Categories
Biotechnology
Medical Device]]>Thu, 23 May 2013 10:28:48 UTCValidation Chemist
Growing Nutraceutical Manufacturer of vitamin supplement ingredients and products is seeking a Chemist to join their team.

Summary
The Chemist is responsible for providing support to Lab Departments, to ensure that all testing is performed in accordance with company written Standard Operation Procedures (SOP), Analytical Procedures, and/or USP/NF Compendia.

Duties and Responsibilities
· Performing wet chemistry, HPLC, GC, Dissolution test, UV, PH.
· Performing analytical tests of raw material, in-process, and finished products.
· Calibrating instruments used for QC testing.
· Documenting test results, problems and other issues, performing initial troubleshooting issues that arise during analysis, conducting all analysis and documentation using GMP and FDA guidelines.
· Investigating OOS issues and implementing corrective actions.
· Performing laboratory instrument validations (IQ, OQ, PQ).
· Performing method validations.
· Performing cleaning validations.
· Other duties, assignments and tasks as assigned by VP or senior management.


Required skills:

· BS Degree in Chemistry (minor in Microbiology) in an accredited college/university; plus
· 5 or more years of work experience performing analytical chemistry in a regulated industry (i.e. Pharmaceutical, Medical Device, Biopharmaceutical, and/or Nutraceutical) and work experience conducting validation (instrument, method, cleaning and process).
· Any combination of experience, education, and training that provides the level of knowledge, skills, and experience needed to successful perform the job.
· Knowledge and understanding of quality in a manufacturing environment, as well as laboratory controls and work safety rules/regulations.

Contact:
CostaMesa@Labsupport.com
Job Type:Employee
Job Status:Full Time
Locations:Multiple Locations
California-Los Angeles
California-Orange County

Categories:Multiple Categories
Food & Beverage
Pharmaceutical]]>Thu, 23 May 2013 10:28:48 UTCMicrobiologist
Our client is a contract manufacturer of liquid and powder nutritional supplements. Being in business for 35+ years, they have recently moved into a large new facility and have multiple openings within their QA department. They are seeking a Microbiologist to join their team.
The Microbiologist will control and assure quality and provide technical support for production by means of microbiological analysis of raw materials, utilities & environment (water, compressed air etc) and finished products.
Responsibilities include:
• Test raw materials and finished products for microbial contamination.
• Assist in trouble shooting production problems.
• Provide assistance in training personnel.
• Prepare and standardize all reagents.
• Calibrate and maintain laboratory equipment.
• Validate procedures used in the micro lab.
• Complete all necessary documentation in microbiology lab to ensure GMP (Good Manufacturing Practices) compliance.
• Other duties as assigned.
Required skills:

Requirements:
• B.S. in Microbiology, Food Science or related field
• 2-5 years of laboratory experience in a pharmaceutical or related industry; 5 year of Quality Control background preferred
• Ability to solve practical problems and carry out responsibilities under general supervision
• Ability to organize workload for effective implementation
• Strong customer and results orientation
• Ability to interact effectively at all levels with sensitivity to cultural diversity
• Ability to function as an effective team member
• Ability to adapt as the external environment and organization evolves

Contact:
costamesa@labsupport.com
Job Type:Employee
Job Status:Full Time
Locations:Multiple Locations
California-Riverside
California-Orange County

Categories:Multiple Categories
Food & Beverage
Personal Care
Pharmaceutical]]>Thu, 23 May 2013 10:28:48 UTCuired.
The successful candidate will be able to perform a variety of laboratory tasks involving data collection, general laboratory upkeep and maintenance, data entry, solution preparation, routine reactor maintenance, instrumentation monitoring, and reactor and instrument troubleshooting. The ability to learn new concepts and new laboratory techniques required.


Required skills:

Minimum of a bachelor’s degree in microbiology, biology, chemistry, engineering, or other similar field preferred. A H.S. diploma with a minimum 2 years of successful work experience in a laboratory environment will also be considered.
· Must be able to follow instructions and procedures pertaining to the task at hand.
· Must be familiar with Windows, MS Office (Word, Excel, Outlook, PowerPoint) and Internet research skills.
· Knowledge of and ability to operate typical laboratory equipment, specifically GC, HPLC, ICP, IC, spectrophotometer and other laboratory equipment a plus.
· Strong organizational and prioritization skills required.
· Attention to detail and accuracy a must. Effective problem-solving skills and the ability to make sound decisions.
· Excellent oral and written skills required. Ability to disseminate information by using the telephone, mail services, Web sites, and e-mail
· Ability to work as a team player in a diverse work group including management, staff, and off-site personnel as well as be able to work independently while alone on shift.
· Strong work ethic.
· Must be able to communicate in English both orally and in writing.
· Must be dependable
Contact:
Dallas Lab Support
Job Type:Employee
Job Status:Full Time
Locations:Multiple Locations
Arkansas - Fayetteville
Arkansas

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:48 UTCor oversees laboratory supply purchases and equipment maintenance; Provides input to budget processes. Performs miscellaneous laboratory duties such as general cleaning, supply management, and waste management.
Required skills:

Bachelor’s degree in Microbiology or Biology or equivalent with a minimum of 3 years related work experience in Cosmetic, Personal Care or Pharmaceutical lab.
Contact:
Dallas Lab Support
Job Type:Employee
Job Status:Full Time
Locations:Texas-Dallas

Categories:Personal Care]]>Thu, 23 May 2013 10:28:48 UTCQA Technician
Lab Support is seeking a Quality Assurance Technician for a Contract (temporary) position in the DFW Area:
§ Conduct microbiological testing of in-process samples and finished goods in accordance with SOP’s and control plan and report results.
§ Work under the guidance of the Packaging Engineer and implement computer-based SPC programs (using Excel, INFINITI QS) to enhance package process control; reduce consumer complaints.
§ Analyze data statistically looking for trends, common and special cause variation. Support continuous improvement initiatives in all areas of the plant.
§ Perform audits on equipment, materials, products and procedures to assure that the lab is in compliance based on CQA (Corporate Quality Assurance) and FSSC / HACCP (Hazard Analysis Critical Control Points) procedures
§ Perform bench-top analysis of critical quality parameters in accordance with SOP’s and control plan. Record data to assure that in-process samples and finished goods are in compliance to specifications.
Required skills:


Pursuing a Bachelor of Science degree in a Business Management or Life Sciences discipline
Excellent skill level with Microsoft Excel and Powerpoint; Minitab skills are preferred.
Very good oral and written communication skills; and ability to analyze technical data to form conclusions / make recommendations
Ability to drive results with minimal supervision
Must be local to the Dallas-Fort Worth area to be considered
Contact:
Dallas Lab Support 972-934-1433
Job Type:Employee
Job Status:Full Time
Locations:Texas-Fort Worth

Categories:Food & Beverage]]>Thu, 23 May 2013 10:28:48 UTCChemistry Technician
Research and development on diagnostic tests including non-invasive glucose testing and development of non-instrumented and instrumented lateral flow assays for infectious agents for decentralized use. The focus will be on optimizing the reagent system for the rapid and accurate quantification of glucose.

Duties and Responsibilities:
• Execute complex experiments, usually involving blood specimen, while adhering to written protocols and safety procedures pertaining to hazardous materials (biological and chemical hazards)
• Work with vendors to expedite parts & supplies with a quick turn-around
• Preparation of buffer and reagents


Required skills:

Required Skills:
• 2-5 years experience in in-vitro diagnostics medical device research and development in an industrial setting or related experiences
• Wet-lab chemistry experience
• Data analysis & graphing using MS Excel
• Experience in general laboratory methods
• Ability to handle human and biological samples including blood
• Mechanical aptitude; ability to work with small parts
• Basic microscope skills
• Mathematical aptitude including familiarity with basic statistical analysis using MS Excel
• Good written and verbal communications skills
• Good observational skills and manual dexterity
• Detail oriented
• Flexible and adaptable with rapidly changing task priorities


Desirable Skills:
• Colormetric assay experience
• Reagent formulation/development/coating/testing experience

Education/Training:
• Associate’s degree or higher plus 1-2 years laboratory experience in Chemistry, Biochemistry, Immunology, Microbiology or related field
Contact:
Denise Gilbrech
Job Type:Contract Hire
Job Status:Full Time
Locations:California-Silicon Valley/San Jose

Categories:Medical Device]]>Thu, 23 May 2013 10:28:48 UTCQA/QC Supervisor
QA/QC Supervisor
Position Classification: Full Time, Exempt
Salary (commensurate with experience and qualifications)
Job Summary:
Reports directly to the Director of Quality and is charged with maintaining a site specific Quality system to assure that all products manufactured by the organization meet customer specifications and achieve superior quality and reliability levels. This includes the supervision of quality technicians as well as technical and scientific support to the operation/production group.
Role and Responsibilities
1. Assist Director in developing, maintaining, and implementing site specific Quality Systems with respect to established internal specifications, cGMP’s, HACCP and USDA regulations.
2. Effectively interact with Production and Development teams to maintain quality of incoming goods and manufactured finished products.
3. Implement and Monitor HACCP program.
4. Perform periodic audits such as Food Safety/Food Security Audits.
5. Monitor Pest Control contractor and program.
6. Maintaining Quality Laboratory results, procedures, equipments, including Calibrations and Verifications.
7. Monitor adherence to product specifications. Disposition of all out-of –spec product and notification of all concerned.
8. Act as a technical resource for operational group regarding product compliance.
9. Monitoring and documenting process and product controls.
10. Maintaining SOP relating to product Quality, Safety and Security.
11. Monitoring plant performance by gathering relevant data and producing statistical reports including customer complaints and out of specification products and processes.
12. Ensuring that all operational management and Corporate Quality notified in the event of out of normal issues.
13. Identifying relevant quality-related training needs and delivering training, including initial and ongoing refresher cGMP, HACCP, Allergens, Food Safety/ Food Security training for employees and contractors as required.
14. Lead investigation and document all non-conformances and site specific customer complaints. Identifying Root Cause and Corrective Actions (CAPA and follow ups).
15. Reporting all site specific Quality KPIs.
16. Ensuring all laboratory tests and calibration procedures are properly understood & carried out.
17. Supervising technical staff in carrying out tests and checks.
18. Writing technical and quality systems reports.
19. Manage and maintain the site’s quality inspection and product release programs for incoming and in-process materials and components, processes and finished goods.
20. Manage the site implementation of corporate quality goals, objectives, policies, procedures and systems pertaining to QA/QC.
21. Maintaining awareness of the business to optimize customer service, including operational schedules to best coordinate Quality efforts to serve customers in a timely manner.
22. Monitoring Plant Sanitation, liaising with sanitation chemical supplier to optimize environmental, process (CIP &COP) product performance.
This will be a 12 hour day shift, with occaional needs for support at other times.
Required skills:

Bachelor’s degree in Food Science, Microbiology, or relatied science with 5 years experience in Quality in the food industry (related cGMP industries will also be considered). Three years managing technician level staff preferred. Flexibility depending on candidate experience will be considered.
Preferred Skills:
Demonstrated written and oral communication skills.
Working knowledge of Microsoft Office-Excel, Word, PowerPoint required, Access desirable.
Experience administering HACCP concepts.
Experience in performing food facility auditing and hosting 3rd party or regulatory audits.
Experience in the Beverage industry as well as food microbiology is a plus.
Work Conditions:
The position is principally performed indoors in a traditional manufacturing setting. Daily activities will include visiting the plant & warehouse facilities. Activities include extended periods of standing, working at a computer monitor and performing laboratory testing using common laboratory reagents. Occasional lifting of products (25-30 lbs)
Contact:
Emma Beatty 602-222-3558
Job Type:Employee
Job Status:Full Time
Locations:Arizona-Phoenix

Categories:Food & Beverage]]>Thu, 23 May 2013 10:28:48 UTCQuality Assurance Technician II
Our client a leader in the Food and beverage industry is looking for a Quality Assurance Technician.
This position coordinates with operations and QA personnel by checking the daily bottling schedule, furnishing and maintaining product specifications, performing routine analyses on incoming raw material, blending and bottling products, maintaining and documenting routine quality systems, and advising supervisors of deviations from the process.
• Performs inspection and testing activities to ensure continuous control over materials, facilities, and products throughout the production cycle.
• Calculates product blends according to required specifications.
• Collects samples of products as needed.
• Maintains and carries out quality assurance objectives complementary to corporate policies and goals.
• Follows company policies and procedures including cGMP, SOP, SSOP, Food Safety/HACCP/SQF or other food safety schemes, GLP, OSHA standards.
• Participates in reviewing and writing SOP, SSOP, food safety procedures and other written materials needed to operate in the lab and processing plant.
• Completes internal audits of the facilities using the above mentioned standards.
• Inspects all job assignments for quality and completion.
• Ensures work is documented properly and timely.
• Performs quality-related, special projects as instructed (i.e. shelf life studies, flavor panels, audits, etc.)
• Acts as the lead person in QA in the absence of a supervisor or manager.
•

Required skills:

Education: High school diploma or GED is required; Undergraduate degree in a basic science is preferred. College-level coursework in food science, chemistry, microbiology, or a related field may be adequate.
Experience: food lab experience is required. Pharmaceutical lab work is adequate.
• Science skills: The person should have a good understanding of basic science – biology, chemistry, microbiology, earth science, physics, or engineering.

If you are qualified please send a copy of your resume
Contact:
Emma Beatty Recruiter Lab Support emma.beatty@labsupport.com
Job Type:Contract Hire
Job Status:Full Time
Locations:Arizona-Phoenix

Categories:Food & Beverage]]>Thu, 23 May 2013 10:28:48 UTCLab Technician
Lab Support is actively recruiting for an Entry Level Lab Technician in North Houston. Our client is a global lubricant company looking to add another technician. Candidates must have a team player attitude and be eager to train. This position is contract to hire.
Required skills:

Candidates with the following skills/background are encouraged to apply:
BS in Biology or AS in Life/Physical Science
Wet Chemistry, titrations, Karl Fischer, ICP and FTIR
Ability to succeed in a fast paced environment
Knowledge of LIMS
Hourly wage is $15.00/hour
Contact:
For immediate consideration, please forward your MS Word resume to: houston@labsupport.com
Job Type:Employee
Job Status:Full Time
Locations:Texas-Houston

Categories:Chemical Industry]]>Thu, 23 May 2013 10:28:47 UTCSenior Research Technician (Leiden)
Our client is a biopharmaceutical company focused on the discovery, development and commercialization of RNA modulating therapeutics. The company targets genetic disorders with a large unmet medical need, with a primary focus on neuromuscular and neurodegenerative disorders. The company has developed a portfolio of clinical and pre-clinical RNA-based drug candidates.

The position
The research technician is responsible for the development of different technologies such as RT-PCR, Western Blotting, immunocytohistochemistry, confocal microscopy and ELISA. Further, you are responsible for writing protocols, compiles, interprets, and documents results, and draws tentative conclusions.
Required Skills:

- HBO Bachelor and/or Masters degree Biochemistry or Molecular Biology
- At least 2 years relevant experience in the industry is required
- You have a strong background in Biochemistry or Molecular Biology and you are familiar with RT-PCR, Western Blotting, immunohistochemistry and ELISA
- Experience in working under quality systems GCLP and GLP is desired
- Good proficiency in English
Contact:
For more information about this vacancy contact Maisi Man (Associate Recruiter) on 030-291 3090. You can send your application to maisi.man@labsupport.nl mentioning reference number 2183764
Job Type:Employee

Job Status:Full Time
LocationsMultiple Locations
Lab Support Netherlands
Lab Support Netherlands

CategoriesMultiple Categories
Biotechnology
Biotechnology]]>Thu, 23 May 2013 10:28:34 UTCQuality Engineering Technician
Job Description –
Bachelor’s Degree in a science-related field required. (Biology, Microbiology, Meat Science, Chemistry, any science-related degree) New Grads welcome!
Monday – Friday 6:00 am – 2:30 pm for 1 to 2 months while training. After that, would either be 5:30 am – 2:00 pm Sunday through Thursday, or Tuesday thru Saturday.
40 hr. week – overtime may be required. Candidate must be able to lift 25 pounds, and be able to travel up and down stairs.

Responsibilities:
• Conduct daily SSOP and HACCP pre-shipment reviews in all departments of the facility.
• Conduct daily Housekeeping auditing in all areas of the facility.
• Perform Quality Line Audits, Warehouse audits, monthly PM’s, water testing, rework evaluation & raw material evaluations, as required.
• Collect in-process and finished product samples, transport samples to lab, and log them into lab SAP database.
• Collect micro and EMP swabs on plant production lines, as required. Lab QS Technicians will prepare/plate and read samples, enter into SAP database.
• Place product on hold by writing Quality Hold tags and/or placing product on electronic hold via the Matrics inventory system.
• Perform Designated Pre-op Inspections (DPI) of production lines after sanitation process is completed to approve line(s) for start-up.
• Professionally manage Quality situations that arise in the plant on off-shifts and weekends as the Quality point person, and must effectively communicate identified issues with production and Quality supervision at all times.
• Lab QS Techs will prep/grind meat samples, perform NIR analysis and wet chemistry analysis (fat, moisture, protein, salt), and enter all analytical data into SAP database.
• Lab QS Techs will also perform package integrity testing (residual air) and perform weekly keeping time evaluations.

Required skills:

Bachelor’s Degree in Science is required. No work study or Visa
• Position requires high level of computer proficiency – Microsoft Excel, Word, Access, PowerPoint, Outlook. Plant database knowledge helpful (SAP, Matrics, Meridian, Internet)
• Must possess very good writing and communication skills. Need to have an approachable personality, be able to deal with conflict and stressful situations appropriately, and have the ability to deliver good and bad news.
• Will be working in team environment. However, needs to be able to work independently.
• Individual is familiar with basic scientific principles and has had some laboratory experience.
• Work experience in a food plant environment is a plus.

Quality and lab experience Past work with food is helpful.

Could be a temp to hire possibility and extension to a year is highly likely.
Contact:
Francis Bauer
Job Type:Contract Hire
Job Status:Full Time
Locations:Iowa-Davenport

Categories:Multiple Categories
Food & Beverage
Food & Beverage]]>Thu, 23 May 2013 10:28:34 UTCLab Technician
Great biorenewables company in need of Lab Technicians to perform analytical testing on samples.
Instrumentation includes: GC, HPLC, IC, IR
Calibration of lab instruments
Wet Chemistry techniques
Data Entry and analysis
Maintain neat and orderly lab environment
Required skills:

BS Biology, Chemistry, Biochemistry, Microbiology or a related science field
Experience in a laboratory setting

This is a long term contract. Pay is $14 an hour
Contact:
Francis Bauer email resume to desmoines@labsupport.com or apply online at www.labsupport.com PH: 515.440.6447
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:Multiple Locations
Cedar Falls, IA
Iowa-Cedar Rapids

Categories:Multiple Categories
Biotechnology
Chemical Industry]]>Thu, 23 May 2013 10:28:34 UTCManager, Product Marketing
Description
The position is responsible for assisting in the development, management, and execution of marketing strategies and tactical programs to effectively achieve commercial objectives for recently approved drug.
Responsibilities
Manage assigned projects related to product marketing including, but not exclusively, the following areas:
Participate in the development of the annual US strategic and tactical marketing plan for product.
Cultivate and maintain relationships with key customers (patients and/or physicians).
Participate in the development and implementation of the US medical communication plan.
Provide input and tactical assistance to the publication plans of product.
Assist in organizing and participate in advisory board meetings with key customers (patient and physician).
Participate in the development and management of an operating budget of the marketing plan.
Obtain feedback from field force to effectively support their efforts.
Evaluate on a continuous basis the efficacy of communications/sales by target audiences to make recommended changes.
Required skills:

Requirements
The successful candidate must possess U.S. in-line pharma/biotech specialty and/or orphan marketing experience (global marketing experience is a plus) of at least 5 years. Product launch experience strongly desired.
Key Skills
Self-starter and highly self-motivated.
Action oriented with strong prioritization skills.
Ability to work well in highly dependent team environment.
Spend effectively within budget (manage budgets).
Ability to evaluate, question, and provide recommendations constructively with appropriate assertiveness.
Strong written and oral communication skills.
Strong analytical skills (ability to draw insights from data).
Education/Experience/Travel
Undergraduate degree in life science or marketing; MBA or M.S. or PharmD is a plus.
Minimum of five years of direct in-line marketing experience. Additional experience in other areas such as field sales, district management, advertising and sales training a plus.
Solid understanding of pharma/biotech marketing, product development and life-cycle management.
Travel will be approximately 20% and predominately in the US
**Please email your resume to jasmine.shu@labsupport.com and use "Product Manager" as the subject title.
Contact:
Jasmine Shu at Jasmine.Shu@labsupport.com
Job Type:Employee
Job Status:Full Time
Locations:California-Marin County/North Bay

Categories:Multiple Categories
Biotechnology
Pharmaceutical]]>Thu, 23 May 2013 10:28:34 UTCResearch Assistant
Job Description:
This position will be accountable for supporting necropsy activities in the Pathology Department. Responsibilities of this position include: Setting up studies, excising tissue samples, fluid collections, administration of compounds required for designated procedures, perfusion techniques, freezing tissues, gross photography, recording organ weights, wet tissue trimming, quality control of work and database entries, ordering and stocking supplies and other general maintenance duties in the Necropsy Lab.
Required skills:

Animal handling and necropsy experience. Manual dexterity for dissection techniques and embedding. Visual acuity to see small details during specimen examinations. Adherence to established policies, procedures and safety requirements. Wet tissue trimming, processing and embedding. Proven technical skills. Strong organizational, communication (both writing and verbal) and interpersonal skills. The applicant must be able to lift 10 lbs.
Education:
< AA or BS degree in animal sciences or similar field and 1-2 years experience with performing the procedures described is required.
Contact:
Jasmine Shu, Jasmine.Shu@labsupport.com and include "Research Assistant" in the subject line.
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:California-Silicon Valley/Peninsula

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:34 UTCResearch Assistant
Job Description:
*********Normal work hours, for at least 1 year.**********
We are seeking a contractor to support drug discovery and development in the Small Molecule Pharmaceutics Group. This position spans responsibilities from the drug discovery stage to early and late clinical trials support. To support projects in the discovery stage, the qualified candidate will provide formulation support for preclinical in vivo studies including PK, PD, efficacy, and tox studies. This person may also conduct preformulation studies and physicochemical characterization to support lead optimization and selection, including salt and polymorph screening. In the development stage, the candidate may assist in the development and characterization of formulations for clinical dosing.
Additional responsibilities include general laboratory managerial duties such as ensuring lab cleanliness and proper waste labeling, ordering and stocking supplies, vehicle and mobile phase preparation.
Required skills:

Strong organizational, communication, and interpersonal skills. Team Oriented, dependable, self starter. Ability to follow detailed verbal and written instruction. Experience with Microsoft Office and lab instrumentation, including analytical balance, pH meter, HPLC, DSC and TGA preferred. Experience in preformulation and formulation of small molecules preferred.
Education:
B.S. in Pharmaceutics/Pharmaceutical Chemistry/Material Science/Chemistry/Biology or related field with 0-3 years of working experience
Contact:
Jasmine Shu, Jasmine.Shu@labsupport.com and include "Research Assistant" in the subject line.
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:California-Silicon Valley/Peninsula

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:34 UTCResearch Associate
Job Description:
We are seeking a Research Associate/Senior Research Associate in the Department of Safety Assessment for conducting and overseeing scientific investigations and screening activities to support discovery and development projects for biological and small molecules.
Main responsibilities will include working in the investigative safety lab to develop new cutting-edge molecular science capabilities to support safety assessment in early drug discovery. There will be a significant component of the selected candidate’s work to be involved in cutting edge stem cell research as well as be involved with large scale collaborative projects. There will be opportunity for developing higher throughput/content molecular expression-based safety assays to differentiate chemical series/targets, and guide project direction and drug design quality; applying molecular-based safety assays to guide structure-activity relationships, differentiate chemotype from target/off-target safety and utilizing chemical and systems biology approaches to evaluate mechanism of action or identify toxic pathways for end organ effects observed in in-vivo preclinical safety studies.
Required skills:

2-3 years of current industrial or academic research experience in molecular toxicology and experience in designing and developing novel higher throughput/content molecular-based predictive toxicity assays required (with particular emphasis on endpoints such as biochemical, anatomical, physiological, imaging/high content, pathological as well as pathway responses, protein phosphorylation, and gene expression).Recent experience with Stem Cell work is highly desirable. A background in cellular biology with strong experience in standard cell culture and molecular biology techniques, transient/stable transfection, cell line engineering, RNA knock-down, protein-protein interactions; and research experience in systems biology or chemical genomics using genomic, proteomic or metabolomic approaches is desirable.
Qualified candidates will have the proven ability to independently design, execute and interpret experiments and proactively apply, qualify and troubleshoot new technologies or assay platforms as needed.
Strong, organizational skills, written and oral communication skills and ability to work on teams are essential.
Education:
Applicant must have a BS/MS in a biological science field.
Contact:
Jasmine Shu, Jasmine.Shu@labsupport.com and include "Research Associate" in the subject line.
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:California-Silicon Valley/Peninsula

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:34 UTCLaboratory Technician/Assistant I
Job Description:
Candidate with experience in techniques that include rodent handling, health monitoring, blood and tissue collection, and dosing via multiple routes.
Required skills:

5-10 years of hands-on experience conducting studies using experimental rodent models.
Basic molecular biology skills required.
Must have strong written and verbal communication skills.
Must be proficient using Excel, Word and PowerPoint.
Must be a strong team player who quickly learns new in vivo techniques.
Must be adaptable and flexible in a fast moving environment.
Possess an AA degree or an equivalent combination of education and experience.
Education:
BA/BS Required
Contact:
Jasmine Shu, Jasmine.shu@labsupport.com, and include "Scientific Associate II" in the subject line.
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:California-Oakland/East Bay

Categories:Pharmaceutical]]>Thu, 23 May 2013 10:28:34 UTCField Service Tech
Field Service Technician will be working in the Long Island, NY area.
The key requirement is the skill and ability to perform mechanical support, troubleshooting, and maintenance on chemical feed pumps, wastewater treatment systems, and electronic handling systems.
We need a motivated self-starter that is capable of following safety procedures when dealing with these systems.
The individual will perform preventive maintenance on pumps, repair pumps when needed, conduct inspections of equipment, and keep equipment systems clean.

Tasks:
Keep chemical feed systems in good working condition.
Be available on short notice to repair systems.
Perform routine maintenance, filter changes, semiannual pump rebuild

Description:
• This is a position for qualified candidates with the skills to support operations at various times at the Water Treatment plant.
• It is estimated that each visit will take 2-3 hours
• It is a long term assignment that can lead to a permanent position.
• You must be computer literate to receive and send files by email and communicate with the hiring manager.


Required skills:


Educational Requirements:

AS in Mechanical Technology, Electronic Engineering Technology, or related

4-5 years of related experiene
This will be a 6-month contract position with the potential to go long-term.
Contact:
Jennifer Ridge 631-249-5190
Job Type:Employee
Job Status:Full Time
Locations:Multiple Locations
New York-Long Island
New York-New York City

Categories:Multiple Categories
Biotechnology
Chemical Industry
Environmental Services]]>Thu, 23 May 2013 10:28:34 UTCVeterinary Services Associate
Looking for a great communicator for an immediate opening with one of our Veterinary Offices for a Veterinary Tech level specialist in an administrative role. Key responsibilities will be helping the veterinarians process lab results, verify reports, document keeping, and answering the phones.
Required skills:

Great Communication is key for this position.
Should have either medical or veterinary technician experience, and have the ability to understand the different terminologies related to the industry. Will also consider medical tech's from a doctor's office setting.
Preferred 6 months -1 year veterinary tech experience.
Apply today, immediately scheduling interviews!
Contact:
Jennifer Ridge 631-249-5190
Job Type:Employee
Job Status:Full Time
Locations:Multiple Locations
New York-Long Island
New York-New York City

Categories:Multiple Categories
Veterinary
Biotechnology
Environmental Services
Medical Device
Personal Care
Pharmaceutical]]>Thu, 23 May 2013 10:28:34 UTCHematology Technologist
We are currently looking for a Medical Lab Technologist with a NYSCL and experience in the Hematology field. The well qualified candidate will be responsible for reading differentials and conducting long-term glucose testing, as well as operating various pieces of equipment.
Required skills:

Candidates MUST have New York State Clinical License in Technology
2-3 years working as a hematologist, or as a generalist with hematology experience of 2-3 years
Should be open to working 2nd or 3rd shift and weekends
We are currently interviewing for this position so apply ASAP to be considered!

Contact:
Jennifer Ridge 631-249-5190
Job Type:Employee
Job Status:Full Time
Locations:New York-Long Island

Categories:Multiple Categories
Biotechnology
Chemical Industry
Clinical Data Management
Materials Science
Medical Device
Pharmaceutical]]>Thu, 23 May 2013 10:28:34 UTCan extensive background in organic and industrial formulation development. The client has a particularly interest in candidates with hair care experience specific to dyes, and a strong organic chemistry background. Fur dye/dressing experience a huge plus.

R&D Formulation Chemist
• HPLC, GC, knowledge a plus to work in Hair Color Research Department. Support Research & Development of Cosmetic formulations.
• Research new products & processes by conducting experiments involving the composition, structure, properties, relationships, & reactions of matter induced by heat, light, & energy.
• Performing formulation of semi-permanent or permanent hair dyes color systems, dye intermediates, and specially formulated bases and developers.
• To provide formulation assistance, new color development, consultation, product line enhancements or help in solving complex dyeing issues for special applications.
• To work with base materials for dyes are cream and liquid formulations designed for maximum color deposition along with superior conditioning.
• Dyestuff and base materials are also available for semi-permanent and specialty systems.
• Develop Cosmetic products & processes by conducting Research, Analysis, Experimentation, & Prior Stability Testing.
• Determine product specifications by studying consumer requirements.
• Determine appropriate & aesthetically pleasing finished products that fulfill requirements of marketability, functionality, and compatibility


Required skills:

• BS or MS; Organic Chemistry background
• Min. 5 year experience in cosmetics industry, preferably in hair care field.
• Extensive knowledge in surfactant chemistry. Have experience formulating cream, liquid, gel cosmetics products.
• Min. Bachelor's degree, prefer Master's of Science in Chemistry or Chemistry related.
• knowledge of hair color formulation a plus
This is an IMMEDIATE opening for a full-time direct hire permanent opportunity.
Contact:
Jennifer Ridge 631-249-5190 longisland@labsupport.com
Job Type:Employee
Job Status:Full Time
Locations:Multiple Locations
New York-Long Island
New York-New York City

Categories:Multiple Categories
Biotechnology
Chemical Industry
Materials Science
Personal Care
Pharmaceutical]]>Thu, 23 May 2013 10:28:34 UTCColor Chemist
Lab Support has an Immediate need for a Part-Time QC Color Chemist in South Jersey!

Seeking chemist/technician to perform QC testing and work on product development of new products.

viscosity
wet chemistry
formulations
pigments, paints, color matching, acrylic paints
Work schedule is 2-3 days per week, working 16-24 hours per week. The position is long term contract/contract to hire.
Required skills:

5 yrs experience in paint and coating industry
degree not required
Contact:
Jessica Berkley 610-660-9830
Job Type:Employee
Job Status:Full Time
Locations:New Jersey-Southern

Categories:Multiple Categories
Chemical Industry
Materials Science]]>Thu, 23 May 2013 10:28:34 UTCQC Chemist
Lab Support has 3 immediate contract QC Chemist Openings in South New Jersey!
This individual would be responsible for performing quality testing on pharmaceutical samples from the production line.
MUST BE FLEXIBLE TO POSSIBLY SWITCH TO ROTATING 12 HOUR SHIFTS
Required skills:

Requirements:
Bachelors degree in Science ( Chemistry preferred)

1-3 years experience in gas chromatography testing and HPLC testing preferred, new top notch college graduate is acceptable

Environmental testing experience using GC and wet chem tests preferred, but not a required
Contact:
Jessica Berkley 610-660-9830
Job Type:Employee
Job Status:Full Time
Locations:New Jersey-Southern

Categories:Pharmaceutical]]>Thu, 23 May 2013 10:28:34 UTCQuality Technician
The primary purpose of this job is to perform instrument assessment testing and data review prior to release of product within the Final Test QC department. Responsible for carrying out product assessment testing complying with GMP and in accordance with procedures. Timely and accurate completion of all related documentation is a key part of the role. Will be responsible for reviewing and approving batch records prior to product release. Will also ensure that the test area and equipment are maintained to a safe and compliant standard.

Key Responsibilities:
Perform QC assessment on ACCESS and UniCel DxI instruments.
Analyze problems / failures, troubleshoot and determine corrective action.
Ensure accuracy and traceability of records to comply with GMP, FDA and ISO requirements. Review and approve instrument batch records.
Generate moderately complex data entry and FPY reports using six sigma / statistical methods.
Initiate changes to current SOPs.
Train other QC technicians or temporary technicians.
Perform other duties assigned by management.
Required skills:

AA degree in mechanical or electrical technician or related field with at least 3 years experience
Proficient with Microsoft Word and Excel.
Basic understanding of six sigma / statistical methods.
Ability to analyze data for trends and/or shifts and work with lead Principle technician to troubleshoot issues.
Knowledge and application of Lean Manufacturing.
Ability to build solid working relationships that enhance collaboration and cooperation with others.
Ability to adapt to changes.
Ability to prioritize daily/weekly work assignments to meet goals.
Ability to communicate effectively within the work unit by gathering and sharing information and/or ideas.
Familiarity with routine instrumentation and laboratory equipment
Ability to multitask and pay attention to detail.
Ability to follow routine procedures without supervision.
Contact:
Jon Swan NRC Recruiter On Assignment, Inc. t: 818-878-3152(x13064)
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:Multiple Locations
Minnesota-Chaska
Minnesota-Minneapolis
Minnesota-St. Paul

Categories:Multiple Categories
Biotechnology
Electronics
Industrial
Medical Device]]>Thu, 23 May 2013 10:28:34 UTCQA Lead Technician
QA Lead for food company
Very hands on position requiring constant contact with prodution, QC, and QA team members
Pull samples from the floor and run QC testing and direct other Qa/QC Technicians
Microbiological testing and data reporting
HACCP knowledge/coordination - lead audits and inspections
Supervise Technicians on 1st shift
Career path position
Computer literate (Word, Excel, others)
Wear multiple hats and don't wait to jump in
SQF 3 knowledge/certification a plus
Reports to corporate QA Manager
Required skills:

BS Degree in Food Science or related industry preferred but not required. 3 or more years working in the Food Industry with some leadership experience strongly preferred.

Contact:
Julie Andersen 602-222-3558
Job Type:Contract Hire
Job Status:Full Time
Locations:Arizona-Phoenix

Categories:Food & Beverage]]>Thu, 23 May 2013 10:28:34 UTCDirector, Quality Assurance and Food Safety
Position Summary: Lead development, implementation/updating, training, management, reporting, documentation, and continuous improvement of product quality, food safety, and related production systems, programs, and activities. Directs activities to insure that ingredients and finished products meet company and customer specifications and that operations are in compliance with all local, state and Federal laws. Manage, educate and coach the QA team, while championing a company-wide culture of product quality excellence.
Essential Duties and Responsibilities:
Establish, implement and maintain/update product and process specifications (Quality Standards) and metrics to monitor product and process performance and assure product quality excellence.
Manage GMP, SSOP and HACCP programs, and implement/manage GFSI (SQF).
Perform/manage self and third-party audits of facilities, processes, raw materials and products; establish, implement and document corrective actions.
Implement and maintain a Vendor Quality Management program, including vendor specifications and audit/oversight requirements.
Investigate, respond to, and document product quality issues.
Regularly report conformance with Quality Standards to Management.
Determine and implement employee training needs related to Quality and Food Safety systems.
Direct quality improvement activities in collaboration with R&D, Operations, Procurement, Customers, and other stakeholders.
Alert and provide guidance to Management regarding quality issues, customer complaints, and related technical matters.
Serve as primary corporate Quality representative and customer liaison in Quality matters.
Act as regulatory agency liaison (with FDA, USDA, state and local agencies in areas of food safety, health, agricultural, and environmental/wastewater compliance); maintain current status of and compliance with related permits, registrations and certifications.
Administer corporate Recall Policy including maintenance of contact database, and act as corporate Recall Coordinator.
Establish strategic plans to improve quality and technical capabilities.
Supervisory Responsibilities:
Directly supervises 5 employees in the Quality Assurance Department.
Carries out supervisory responsibilities in accordance with the organization's policies and applicable laws.
Responsibilities include interviewing, hiring, and training employees; planning, assigning, and directing work; appraising performance; rewarding and disciplining employees; addressing complaints and resolving problems.
Core Competencies: In order to succeed in this position, an individual must exhibit the following core competencies:
Knowledgeable of biology, chemistry and analytical methods for evaluating juice/beverage product quality and safety.
Knowledgeable of US food laws and juice/beverage manufacturing methods.
Capable of working as a member of a multi-disciplinary team in multiple production locations to assure products meet customer specifications and safety requirements.
Capable of designing work flows and procedures and directing a technical quality assurance staff in multiple production locations.
Work Environment:
While performing the duties of this job, the employee may be frequently exposed moving mechanical parts and forklifts, airborne particles, and outdoor weather conditions.
The employee is occasionally exposed to wet or humid conditions (non-weather).
The noise level in the work environment may be loud.
The employee is occasionally required to stand; walk and sit.
The employee may occasionally be required to lift and/or move up to 50 pounds.
Required skills:

Education: Bachelor's degree (B. S.) from four-year college or university, majoring in food science or a related field; MS degree preferred.
Experience: Minimum ten (10) years progressive experience in Quality Assurance/Control in the food industry
Personnel management experience, preferably in a multi-location environment.
HACCP certification required; GFSI (SQF practitioner) and/or ASQ Auditor certification strongly preferred
Detailed working knowledge of FDA and USDA regulations, Good Manufacturing Practices, sanitation, pest control, and food allergens.
Proficiency with statistical process control, pasteurization and related processes, QA laboratory equipment, analytical/microbiological testing methodologies, and knowledge of sensory and shelf-life evaluation techniques
Language/Communications: Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations. Ability to write reports, business correspondence, and procedure manuals. Ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public.
Reasoning: Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables.
Computer Skills: To perform this job successfully, an individual should have knowledge of Word Processing software; Spreadsheet software; Manufacturing software; and general email writing and online research skills.

Contact:
Julie Andersen 602-222-3558
Job Type:Employee
Job Status:Full Time
Locations:Arizona-Phoenix

Categories:Food & Beverage]]>Thu, 23 May 2013 10:28:34 UTCChemical Engineer
• Work independently and with operators to perform experiments in support of process development activities
• Input and monitor process control and product quality data to track performance, interpret data, and identify trends
• Coordinate and assist in the execution of non-standard production of nanocrystals using new process parameters, materials, and equipment.
• Establish draft operational procedures and support roll out training to the work force.

Required skills:

Education and Experience:
• A minimum of an Associates degree in chemistry or engineering
• Three years of experience as an R&D or Engineering process technician in a chemical manufacturing operation.
• Chemical Engineering or Chemistry B.S strongly preferred.
• Hands on experience working with chemicals in a laboratory or manufacturing environment and solid knowledge of the associated safety requirements for such work.
Other Skills and Abilities:
• Strong written/verbal communication skills are required in order to deliver information to operators, engineers, and management.
• Strong decision-making and organizational skills are very important.
• Proficient in the use of basic computer driven test systems and manual measurement tools.
• Proficient in basic algebraic calculations.
• Ability to perform unit conversion calculations.
• Familiar with basic chemical property terms and calculations (density, moles, mass, volume, % composition).


Contact:
Kimberly Plum
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:Maryland-Baltimore

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:33 UTCNMR Chemist
The NMR Chemist will be responsible for the operation and management of four NMR spectrometers for a state-of-the-art research facility that offers scientific services and instruments to faculty, academic, government and industry researchers. As the key person in the NMR group, you will be responsible for the technical maintenance of the spectrometers, (including cryogen fills) troubleshooting, training and assisting students, faculty and external users. Collect routine NMR data as a service, assist users and answer questions. Manage orders and schedule using CRF database. Provide facility tour and outreach.
Required skills:

Education: B.Sc. degree in chemistry, chemical engineering or a related field (M.Sc. preferred) with at least two years demonstrated experience in either one or both high resolution or solid state NMR spectroscopy.
Experience in for both liquid and solid state analysis desired. Enthusiastic, highly motivated and work well both independently and in groups. Excellent interpersonal skills, team player.
Contact:
Kristin O'Brien
Job Type:Employee
Job Status:Full Time
Locations:Massachusetts-Boston North

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:33 UTCQC Senior Analyst
We are seeking an outstanding candidate that will be responsible for the management of QC testing functions at contract laboratories and contract manufacturers for late stage clinical development programs.

Key Responsibilities:

- Maintains a strong relationship with contract organizations to ensure our colleagues are aligned with Quality expectations
- Manages transfers and validations for in-process and release testing methods at contract sites
- Reviews in-process and release testing results from contract laboratories in conjunction with batch disposition
- Manages stability testing and data trending• Collaborates to support deviations and investigations associated with testing
- Manages test methods and specifications for drug substance, drug product, components and raw materials • Authors QC sections of regulatory filings
Work Environment: Office
- Some travel required
Required skills:

- BS in Chemistry, Biology or Life Science discipline
- 6+ years of experience in GMP Laboratory or Quality role within the biotech or pharmaceutical industry
Preferred Qualifications and Experience:
- Knowledge of ICH, FDA, CFR requirements for development programs
- Excellent organizational and analytical skills, and attention to detail
- Ability to manage multiple and varied tasks, and prioritize workload
- Excellent written and verbal communication skills
- Experience with Microsoft based applications
- Laboratory experience in quality control or analytical development, including HPLC
- Experience working with external contract organizations
- Experience in developing and writing procedures, protocols, and regulatory documentsCompetencies
- Results Orientation - model a strong work ethic and persevere to achieve results, consistently follow through on your work promises
- Problem Solving - apply your background and experience to recognize patterns and potential solutions, when evaluating possible solutions to problems, understand multifunctional interdependencies and causal relationships
- Promotes Teamwork - You understand how your role interacts with others' roles, think beyond your function in an enterprise-wide manner, create a trusting relationship with colleagues
- Effective communication - express ideas and information clearly and accurately, including speaking and writing concisely and clearly, proactively and tactfully addressing concerns with others when problems persist.
Contact:
Kristin O'Brien
Job Type:Employee
Job Status:Full Time
Locations:Massachusetts-Boston

Categories:Pharmaceutical]]>Thu, 23 May 2013 10:28:33 UTCAssociate Biosample Support Coordinator
Job Description:
**To be considered for this position, all candidates must have a Pathology background.**

Pre-Study activities (working under the direction of the Manager or Senior Coordinator):
Review draft protocol for sample related issues (number of subjects, number of aliquots, sample type, etc.)
Collaborate with Clinical Operations to prepare Scope of Work document for Central Lab-run studies.
Forward any necessary supplies to sites participating in trials.
On-Going Study Activities:
Receive study samples via the GNE receiving dept.
Inventory shipment, reconcile any sample discrepancies with study team and log samples into the
Electronic Sample Tracking System (ESTS) with guidance from superiors.
Prepare samples for assay based on study needs and update the ESTS.
Deliver samples to the appropriate assay group.
Archive samples returned from the assay group, or if appropriate, for future additional research.
Follow user manuals and system SOPs with supervision.
Follow appropriate GXP guidelines.
Meet all study timelines.
Maintain a neat working environment in laboratory work areas.
Maintain an adequate level of supplies.
Create simple study related ad hoc reports for customers.
Required skills:

Proficiency with PC computer systems, including email and calendar applications.
Basic understanding of relational database concepts and SQL query scripts.
Proficiency with MS Office applications.
Basic skill level with web page authoring for modifying or creating simple web pages.
Strong organizational, communication, multitasking, and prioritization skills.
Strong written and oral communication skills.
Ability to follow verbal and written instructions from superiors.
Requires attention to detail and accuracy in data entry while maintaining study timelines.
Strong analytical and problem solving skills, paired with partnering and performance skills.
Team player with demonstrated strong interpersonal skills and ability to build effective working relationships within functional area.
Education:
Minimum BA/BS or AS in life sciences or appropriate training and experience. Pharmaceutical/Biotech industry experiences a plus.
Contact:
Lindsay Schulz, lindsay.schulz@labsupport.com and include "Associate Biosample Support Coordinator" in the subject line.
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:California-San Francisco

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:33 UTCAssociate Scientist
Job Description:
The temporary research scientist will participate in the bio-therapeutic drug discovery process at Genentech. The candidate will apply quantitative mass spectrometry techniques for protein therapeutic quantification. He or she will develop protein and peptide sample preparation methods suitable for mass spec analysis and utilize proteomic and bioinformatics software tools for data analysis. Practical experience in the design, development, validation and execution of mass spectrometric methods for peptide and intact protein using triple quadrupole and/or Q-Tof is required; experience with developing cellular assays is a plus.
Required skills:

The candidate should have experience in proteomics and intact protein mass spectrometry characterization; experience in development of cellular assays is a plus. The ideal candidate will have practical experience in various mass spectrometry instruments, and should be familiar with the typical workflow of data analysis. Familiarity with automated or semi-automated instrumentation is advantageous. The position requires good communication skills and the ability to work well as part of a team. It also requires excellent time management and organizational skills.
Education:
The qualified individual will possess a Ph.D. degree in an analytical science with 5+ years experience in mass spectrometry applications in the biological sciences.
Contact:
Lindsay Schulz, lindsay.schulz@labsupport.com and include "Associate Scientist" in the subject line.
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:California-San Francisco

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:33 UTCAssociate Tech Editor Writer
Job Description:
Train on STATURE risk management tool.
Locate, format and import existing Quality Risk Management Excel files into STATURE risk management tool.
Required skills:

Working proficiency using Excel. Strong attention to detail and excellent proofreading skills . Ability to work independently. Ability to prioritize and organize diverse workload to meet required timelines. Prior experience with GMP document management is a plus.
Education:
College degree preferred, but not required.
Contact:
Lindsay Schulz, lindsay.schulz@labsupport.com and include "Associate Tech Editor Writer" in the subject line.
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:California-San Francisco

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:33 UTCManufacturing Technician
Job Description:
******Technicians will be working alternating Wednesdays, Thursday-Saturday 07:00am-8:00pm*******
This position will be responsible for the aseptic processing of Pharmaceutical components and products using cGMP standards while maintaining the production schedule. Job responsibilities include, but are not limited to: Adhere to SOPs, cGMPs, plant safety guidelines and other established procedures during the manufacturing process to produce quality product Accurately complete and maintain detail oriented process-related documentation of equipment logs and batch histories in a timely manner following the good manufacturing documentation practices Adopt and maintain a team work attitude to effectively and efficiently manage production needs within the Commercial Filling Department. Aseptic processing filtering and filling of pharmaceutical products Environmental monitoring of manufacturing facility Shipping and receiving product Setup, operation, and basic troubleshooting of production equipment Perform manual cleaning and sterilization of parts and components Operate autoclaves for preparation of sterile components CIP/SIP tanks and parts Vial washing, capping, traying of product Able to work flexible hours and overtime.
Required skills:

Perform basic mathematical calculations Lift 25-30 lbs and work extended hours while standing Strong verbal and written communication Ability to follow detailed verbal and written instructions Strong interpersonal skills Passion for learning, dependable, self starter, organized and strong time management skills Proficient with PC Desktop and applications Must pass Aseptic Medical Exam cGMP experience, Aseptic processing, and clean room experience preferred.
Education:
Qualified candidates will possess a degree in Life Science or equivalent combination of education and relative work experience. Prior experience in a biotech, pharmaceutical, or chemical manufacturing environment preferred.
Contact:
Lindsay Schulz, lindsay.schulz@labsupport.com and include "Manufacturing Technician" in the subject line.
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:California-San Francisco

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:33 UTCManufacturing Technician
Job Description:
This position will be responsible for the aseptic processing of Pharmaceutical components and products using cGMP standards while maintaining the production schedule. Job responsibilities include, but are not limited to: Adhere to SOPs, cGMPs, plant safety guidelines and other established procedures during the manufacturing process to produce quality product Accurately complete and maintain detail oriented process-related documentation of equipment logs and batch histories in a timely manner following the good manufacturing documentation practices Adopt and maintain a team work attitude to effectively and efficiently manage production needs within the Commercial Filling Department. Aseptic processing filtering and filling of pharmaceutical products Environmental monitoring of manufacturing facility Shipping and receiving product Setup, operation, and basic troubleshooting of production equipment Perform manual cleaning and sterilization of parts and components Operate autoclaves for preparation of sterile components CIP/SIP tanks and parts Vial washing, capping, traying of product Able to work flexible hours and overtime.
Required skills:

Perform basic mathematical calculations Lift 25-30 lbs and work extended hours while standing Strong verbal and written communication Ability to follow detailed verbal and written instructions Strong interpersonal skills Passion for learning, dependable, self starter, organized and strong time management skills Proficient with PC Desktop and applications Must pass Aseptic Medical Exam cGMP experience, Aseptic processing, and clean room experience preferred.
Education:
Qualified candidates will possess a degree in Life Science or equivalent combination of education and relative work experience. Prior experience in a biotech, pharmaceutical, or chemical manufacturing environment preferred
Contact:
Lindsay Schulz, lindsay.schulz@labsupport.com and include "Manufacturing Technician" in the subject line.
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:California-San Francisco

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:33 UTCQA Analyst I
Job Description:
******Possible Extension*******
Follow company policies and procedures.
Maintain a state of inspection readiness.
Provide input to the development of personal performance goals and departmental objectives.
Collaborate with Management to establish and meet targets and timelines.
Independently manage competing priorities with limited instruction.
Serve as a Quality representative on cross-functional and multi-site teams.
Identify and recommend solutions to potential procedure, process and system gaps.
Provide assistance to customers in support of departmental functions.
Participate in the design and implementation of department and cross-functional initiatives. Apply basic theory and technical principles to address moderately complex problems. Troubleshoot and initiate the resolution of Quality issues by fostering effective interdepartmental and cross-functional partnerships.
Be accountable for behaviors as described in Genentech’s Core, Common, and Critical Competencies.
Perform any other tasks as requested by Management to support Quality oversight activities.
Review and approve controlled documents relating to processes, equipment, facilities and utilities in the manufacture of product. Represent Quality Assurance on multi-disciplinary project teams.
Review and approve change requests.
Assist with discrepancy investigations.
Interact with interdepartmental contacts on discrepancy assessment, resolution, and quality approval.
Assist with manufacturing facility and equipment start-up/changeover/tooling activities.
Administer the change control and discrepancy management programs, ensuring that each program is consistent with current regulatory and industry guidelines.
Provide Quality oversight to internal and external customers.
Collaborate with departments to ensure that all review activities are executed efficiently and effectively.
Required skills:

Knowledge of cGMPs or equivalent regulations strongly preferred
Ability to interpret Quality standards for implementation
Ability to independently evaluate situations and propose potential solutions
Ability to interpret Quality standards for implementation
Ability to communicate clearly and professionally both in writing and verbally
Education:
B.A. or B.S. degree (preferably in Life Science) and at least two years experience in the pharmaceutical, biopharmaceutical or related industry, or an equivalent combination of education and experience
Contact:
Lindsay Schulz, lindsay.schulz@labsupport.com and include "QA Analyst I" in the subject line.
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:California-San Francisco

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:33 UTCQA Specialist III-Quality and Compliance Lead
Job Description:
*************There is a possibility the assignment will be extended.********************
The Quality and Compliance Lead has an advanced knowledge base regarding Operational Quality. This position is responsible assisting in the maintenance of all aspects of quality and general compliance within the Access Solutions Organization, and the management of external business partners. Additional key responsibilities of this role are: quality implementation and management, general compliance mitigation, cross-functional and multilevel partnership, represents the Assess Solutions Organization as a subject matter expert on compliance related matters.
Identify and address quality enhancements.
Share responsibility for monitoring, review and analysis of quality tactics
Assists in the integration of quality and general compliance to address complex problems; provide communications to business partners.
Provide verbal and written communication to internal and external partners regarding clear and concise quality and compliance guidance within context.
Deliver well organized presentations
With limited oversight, develop resolutions to complex quality issues, impacted goals, and the objectives of business partners.
Act as a team member for quality/compliance questions. Represent Access Solutions on project teams, and multi-disciplinary groups
Interact with business partners on quality and compliance matters of low to medium risk.
Required skills:

Minimum of 3-5 years experience in the pharma/biotech industry or in an equivalent setting or relevant and related experience.
Minimum 2 years experience in auditing or Operational Quality Excellence in a call center environment
Must be a strategic thinker who keeps abreast of new developments in quality and continuously improves proficiency
Excellent written and oral communication skills, with a proven ability to communicate effectively across leadership levels.
Demonstrate commitment to uphold Access Solutions values and vision regarding quality and compliance
Strong meeting management and group process facilitation skills, with ability to structure small and large-group meetings to achieve pre-defined objectives.
Strong customer service orientation.
Team player with demonstrated strong interpersonal skills and ability to build effective working relationships throughout all levels of the organization
Approaches work with energy and a positive, constructive attitude
High competency in the following areas: priority setting, multi-tasking, planning, process and project oriented, strategic ability, organizational agility, effective decision making, results oriented, time management, ability to work under pressure and with tight deadlines.
Education:
Bachelors Degree (in a science related field)
Masters Degree in business or health sciences, preferred
Contact:
Lindsay Schulz, lindsay.schulz@labsupport.com and include "QA Specialist III" in the subject line.
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:California-San Francisco

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:33 UTCQC Analyst I
Job Description:
Responsible for general support activities for a GMP testing laboratory including:
- Small equipment maintenance and calibration (logbook verification, maintenance, etc.)
- Maintain temperature monitoring units
- Various administrative duties to support the laboratory such as ordering of chemicals and supplies
- Routine maintenance of the lab to ensure compliance with cGMP, GLP and safety regulations
- Support Quality Control sample management process (sample handling and internal transfer within QC)
- Reagent preparation
- Support routine and non-routine analysis of pre-clinical and clinical products
Required skills:

The candidate must have excellent verbal and written communication skills, organizational skills; is detailed-oriented, and has the ability to work
effectively in a fast paced, multi-disciplinary team environment with various projects and timelines. Hands-on experience with or knowledge of UV
spectrophotometry, Osmolality, pH and other general wet chemistry or chromatography assays is a plus. Experience in a cGMP environment is a plus.
Education:
B.S. in Chemistry, Biochemistry or related field.
Contact:
Lindsay Schulz, lindsay.schulz@labsupport.com and include "QC Analyst I" in the subject line.
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:California-San Francisco

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:33 UTCResearch Assistant
Job Description:
The Research Asst will support Genentech development projects by performing assays. S/he will handle biohazardous, cytotoxic, and adhere to corporate safety standards in all aspects of the work. S/he will use automated liquid handling systems and robotic systems, and will analyze data and report results using specialized software in multiple assay methodologies. S/he will maintain GLP/GCP compliance in supporting clinical and nonclinical studies, and will apply thorough and accurate documentation skills.
Required skills:

Strong organizational, communication, interpersonal skills, team oriented, dependable, and self starter. Ability to follow detailed verbal and written instruction. Able to apply analytical skills and judgment in assessing the quality of assay data and assay performance. Must be self-motivated, able to multi-task, and meet timelines efficiently and productively. Experience preferably in a testing environment that includes ELISA and cell based assays knowledge.
Education:
BA/BS/MS or equivalent experience
Contact:
Lindsay Schulz, Lindsay.Schulz@labsupport.com and include "Research Assistant" in the subject line.
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:California-San Francisco

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:33 UTCResearch Assistant
Job Description:
A temp position in the purification group of Protein Chemistry Department to support on-going research projects in Genentech. The candidate will be working as part of a team that focuses on the purification and characterization of recombinant proteins produced in bacteria, baculovirus insect cells and mammalian cells. Responsibilities include carrying out cell lysis and several purification procedures that include affinity, ion exchange, size exclusion chromatography and RP-HPLC. The candidate will use AKTA liquid chromatography systems, and will characterize purified proteins using SDS-PAGE gels, mass spectrometry, light scattering and circular dichroism. Detailed documentation will be employed. Experience in refolding of denatured proteins from E coli is a plus.
Required skills:

Strong organizational, communication, and interpersonal skills. Team oriented, dependable, self starter. Ability to follow detailed verbal and written instruction. The candidate will preferably have 1-3 years of demonstrated work with proteins. Candidate must be highly motivated, like working in a team environment and have strong interpersonal capabilities. Must be self-motivated, able to multi-task, and meet timelines efficiently and productively. Strong verbal communication, writing, and listening skills, as well as interpersonal skills required.
Education:
BA/BS/MS or equivalent experience
Contact:
Lindsay Schulz, lindsay.schulz@labsupport.com and include "Research Assistant" in the subject line.
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:California-San Francisco

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:33 UTCs in research and early development. Responsibilities will include developing and performing immunoassays (ELISAs) and cell-based bioassays. The candidate may conduct in vitro experiments with cell lines and/or plasma samples, and may work with cytotoxic materials. Thus familiarity with cell culture and biological sample laboratory safety standards will be required. S/he will use automated liquid handling systems and robotic systems, and will analyze data and report results using specialized software in multiple assay methodologies.
Required skills:

Experience with immunoassays (ELISAs) and cell culture are required. At least 2 years lab experience required. The candidate should be able to apply analytical skills and judgment in assessing the quality of assay data and assay performance. Must be self-motivated, detail oriented, and able to multi-task and meet timelines efficiently and productively. Strong verbal and written communication skills, listening skills, and interpersonal skills are required.
Education:
A Bachelor’s or Master’s degree in the Sciences
Contact:
Lindsay Schulz, lindsay.schulz@labsupport.com and include "Research Associate" in the subject line.
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:California-San Francisco

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:33 UTCResearch Associate
Job Description:
*******End date is flexible********
Selected candidate will work in cell line development group within early stage cell culture to provide support of delivering candidate cell lines for clinical trials and commercial manufacturing. Primary responsibilities include cell culture maintenance, new method development, and data analysis with guidance. The candidate is expected to maintain and screen multiple CHO cell cultures in various vessels including but not limited to well plates and shake flaks. The candidate will sample and submit for assays and analyze data as needed. The candidate will also be expected to support simple throughput work as well as routine maintenance of instruments in the laboratory.
Required skills:

Must have extensive hands-on experiences with cell culture/aseptic techniques.
Must have strong motivation to learn.
Must be flexible to handle throughput work and to meet timelines and willing to work in a dynamic and fast-paced working environment.
Must have good communication, multi-tasking, and problem solving skills.
Ability to handle and analyze extensive data is desirable.
Basic knowledge in cell biology and molecular biology is desired
Education:
B.S. degree with at least 4 years lab experience or M.S. degree 2 years of experience
Contact:
Lindsay Schulz, lindsay.schulz@labsupport.com and include "Research Associate" in the subject line.
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:California-San Francisco

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:33 UTCResearch Associate
Job Description:

The temporary research associate will participate in the small molecule drug discovery process at Genentech. The temporary research associate will ensure successful completion of recording, analysis, verification, and presentation of assay results. The candidate will apply their knowledge of enzyme kinetics and biochemical assay development to prepare and validate rigorous assays suitable for characterizing the potency and MOA of small molecule inhibitors. The candidate will have the opportunity to conduct detailed data analyses and will present these data to project teams and senior management. Practical experience in the design, development, validation and execution of biochemical assays in microplate format is required; experience with developing cellular assays is a plus. Experience with data analysis methods and software, including automated dose-response measurements, is required. Familiarity with automated or semi-automated instrumentation would be advantageous, as would familiarity with the multi-disciplinary activities of hit profiling. The position requires good communication skills and the ability to work well as part of a team. It also requires excellent time management and organizational skills.
Required skills:

Practical experience in the design, development, validation and execution of cellular assays in microplate format is required; experience with developing biochemical assays is a plus. Experience with data analysis methods and software, including automated dose-response measurements, is required. Familiarity with automated or semi-automated instrumentation, while not required, would be advantageous, as would familiarity with the multi-disciplinary activities of hit profiling. The position requires good communication skills and the ability to work well as part of a team. It also requires excellent time management and organizational skills

Education:
The qualified individual will possess a B.S. and at least 5 years of relevant experience preferably in the biotechnology or pharmaceutical industry.
Contact:
Lindsay Schulz, lindsay.schulz@labsupport.com and include "Research Associate" in the subject line.
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:California-San Francisco

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:23 UTCResearch Associate
Job Description:
The temporary research associate will participate in the small molecule drug discovery process at Genentech. The temporary research associate will ensure successful completion of recording, analysis, verification, and presentation of assay results. The candidate will apply their knowledge of cellular assay development to prepare and validate rigorous assays suitable for characterizing the potency of small molecule inhibitors in cells. The candidate will also support routine PD immunoassays. The candidate will have the opportunity to conduct detailed data analyses and will present these data to project teams and senior management. Practical experience in the design, development, validation and execution of cellular assays in microplate format is required; experience with developing biochemical assays is a plus. Experience with data analysis methods and software, including automated dose-response measurements, is required. Familiarity with automated or semi-automated instrumentation would be advantageous, as would familiarity with the multi-disciplinary activities of hit profiling. The position requires good communication skills and the ability to work well as part of a team. It also requires excellent time management and organizational skills.
Required skills:

Practical experience in the design, development, validation and execution of cellular assays in microplate format is required; experience with developing biochemical assays is a plus. Experience with data analysis methods and software, including automated dose-response measurements, is required. Familiarity with automated or semi-automated instrumentation, while not required, would be advantageous, as would familiarity with the multi-disciplinary activities of hit profiling. The position requires good communication skills and the ability to work well as part of a team. It also requires excellent time management and organizational skills
Education:
The qualified individual will possess a B.S. and at least 5 years of relevant experience preferably in the biotechnology or pharmaceutical industry.
Contact:
Lindsay Schulz, lindsay.schulz@labsupport.com and include "Research Associate" in the subject line.
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:California-San Francisco

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:23 UTCResearch Associate
Job Description:
The position: We are seeking a highly motivated, enthusiastic, an independent Research Associate/Senior Research Associate to join the Clinical Pharmacology Group in the Department of Development Sciences. Responsibilities: The candidate will provide technical support for the pharmacokinetic and pharmacodynamics assessment of drug candidates and marketed products. The overall scope and focus of this position is to support pharmacokinetic analyses, which seek to optimize dose regimens and strategies to facilitate clinical development and regulatory approval as well as post-marketing commitments. In addition, the candidate will effectively collaborate with e colleague in data programming, biostatistics, and/or infrastructure to facilitate the timely preparation and transfer of data sets containing PK/PD and critical patient demographic and treatment data for analyses. The successful candidate may be expected to represent his/her functional area at team meetings to present data, contribute to the writing of study reports and documentation that support regulatory filings, and to work independently or under the direct supervision of a Scientist.
Required skills:

Who you are: Have 2 or more years of relevant experience in pharmacokinetic analysis, preferable in the Biotechnology or Pharmaceutical Industry, organizing data for presentations and study reports. Senior Research Associate will require a minimum of 8 years of industry experience. Experience in pharmacokinetic modeling preferred. Strong analytical, organization, and communication skills, attention to detail, as well as working effectively in a multidisciplinary team setting are essential.
Education:
A BA or BS in Statistics, Mathematics, Biology, Chemistry or other scientific field is required (MS is a plus).
Contact:
Lindsay Schulz, lindsay.schulz@labsupport.com and include "Research Associate" in the subject line.
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:California-San Francisco

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:23 UTCSenior Research Associate
Job Description:
Research Associate/Sr Research Associate—Investigative Safety Assessment
The Department of Safety Assessment at Genentech provides scientific leadership in the areas of toxicology and toxicologic pathology and plays an active role in the process of drug development from discovery through marketed products.
Responsibilities:
We are seeking a Research Associate in the Department of Safety Assessment to support drug discovery and development. The qualified candidate will work closely with toxicologists and pathologists to investigate mechanisms of toxicity utilizing in-vitro and in-vivo models.
The successful candidate will be responsible for developing, optimizing, qualifying and executing biochemical and cellular assays to investigate the molecular pathogenesis of identified toxicology issues in our South San Francisco location.
Required skills:

Applicants should have a BS or MS in neurobiology, cellular and molecular biology, toxicology, or related field. At least 3-5 years of relevant research experience in the development and execution of enzyme and/or cell-based assays in a variety of different formats, and advanced knowledge of cell isolation and culturing techniques and hands-on experience with relevant state-of-the-art molecular biology techniques (e.g. RT-PCR, Western Analysis, ELISA, and reporter assays). Experience in electrophysiology, FACS and immuno histochemistry is desirable. Qualified candidates will have the proven ability to independently design, execute, interpret experiments and troubleshoot as needed. Strong, organizational skills, written and oral communication skills and ability to work on teams are essential.
Education:
Applicants should have a BS or MS in neurobiology, cellular and molecular biology, toxicology, or related field. At least 3-5 years of relevant research experience
Contact:
Lindsay Schulz, lindsay.schulz@labsupport.com and include "Senior Research Associate" in the subject line.
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:California-San Francisco

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:23 UTCValidation Engineer-Testing
Job Description:



Supporting IQ, OQ, and PQ Testing Activities…
Prior experience in a GMP and/or GLP environment
Strong organizational skills
Proficiency in both reading and writing comprehension
Ability and willingness to support routine operations
Clear and professional communication, both written and verbal
Capacity for meeting targets within specified timelines
Understanding of the need to strictly follow SOPs and Protocols
Prior experience with technical writing
Task-Specific Requirements:



Experience with data analysis, reporting of results per validation protocols.
Experience with authoring SOPs, Protocols and/or summary reports
Ability to identify and author deviations to documented operational practices
Experience with V2K Validators and thermocouples
Prior equipment qualification and/or commissioning experience
Knowledge of proper handling of biological indicators and/or endotoxins
Prior experience with SIP systems
Prior experience with mixing studies
Required skills:

3+ years experience
Education:
BS in Life Sciences mandatory ; Engineering preferred
Contact:
Lindsay Schulz, lindsay.schulz@labsupport.com and include "Validation Engineer-Testing" in the subject line.
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:California-San Francisco

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:23 UTCAssociate Research Scientist I
Job Description:
This individual will perform microbial fermentations to produce recombinant proteins using soluble and insoluble expression systems.
These efforts will be towards scale down characterization studies to support Validation efforts and Manufacturing process.
Novartis Diagnostics is seeking a highly motivated individual with proven abilities who will be involved in the execution and analysis of upstream fermentation experiments.
We expect the successful candidate to contribute to the group by collaborating with colleagues to support company goals.
The incumbent will rigorously document work in laboratory notebooks and summarize work in presentations.
Required skills:

Experience operating microbial fermentors and using fermentation software packages
Ability to plan and execute basic protocols such as flask experiments
Mechanical Aptitude and ability to trouble shoot processes and equipment.
A flexible schedule with the ability to do some shift work and availability on weekends.
Experience performing basic analytical protein techniques (SDS-PAGE, HPLC and Western Blot).
Excellent, up to date recordkeeping.
Ability to work in a fast-paced team environment.
Excellent verbal and written communication skills.
Capable of working with limited supervision on multiple projects.
Proficiency in MS Word, Excel, and Powerpoint.
Experience with statistical software packages a plus
Commitment to laboratory safety practices and hygiene.
Education:
B.S. degree in biological or chemical sciences plus a minimum of 1-5 years relevant industrial experience
Contact:
Lindsay Schulz, Lindsay.Schulz@labsupport.com, and include "Associate Research Scientist I" in the subject line.
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:California-Oakland/East Bay

Categories:Pharmaceutical]]>Thu, 23 May 2013 10:28:23 UTCQuality Assurance Associate
Lab Support now has an urgent need for a Quality Assurance Analyst at our client's Pittsburgh Location
Targeted salary - $35,000-$45,000/yr
Summary of Essential Job Functions:
• The incumbent will be responsible for performing compliance reviews of the batch records for both in-house and externally manufactured product including in-process testing results, final QC release testing results, labeling/ packaging, and all supporting documentation.
• Reviews completed analytical data for conformance to regulations, SOPs, specifications, and other applicable acceptance criteria.
• Reviews, edits, and approves deviation notifications & investigations, and corrective actions.
• Reviews, edits, and approves change control SOPs.
• Reviews, edits, and approves new and revised master manufacturing records.
• Audits production and other departments for quality system effectiveness.
• Performs hands-on monitoring of production and non-production activities and notifies area and Quality Management of any observed non-compliance.
• Perform component acceptance activities.

Required skills:

• Candidates for this position must have at least 1 year direct QA experience in a GMP/ Clinical manufacturing in the biotech industry with increasing responsibilities.
• Previous experience with internal and vendor audits.
• Regulatory Affairs experience is a plus.
Abilities Required:
• Looking for a strong knowledge of word processing, spreadsheet, and databases.
• Ability to interpret applicable standards and objectively make decisions.
• Knowledge of c GMP pharmaceutical / medical device regulations.
• Knowledge of inventory control processes.
• Self motivated and able to work independently.
Contact:
Lisa Conley
Job Type:Employee
Job Status:Full Time
Locations:Multiple Locations
Pennsylvania-Harrisburg
Pennsylvania-Pittsburgh
Pennsylvania-York/Lancaster

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:23 UTCResearch Technician
Lab Support now has an immediate need for a Research Technician
Responsibilities:
· Tissue Culture
· Aseptic technique and proper handling of human tissue/ cell specimens
· ELISA
· Protein quantification

Prerequisites include a strong background in biochemistry or biological science and methodology. The candidate will run and develop cellular assays using human-derived cells, as well as molecular assays involving PCR and enzyme kinetics. Cell culture experience is essential and hands-on experience performing ELISA’s and Flow Cytometry is desired. A Background in formulation of hydrogels and extracellular matrices is desirable.
Required skills:

Education: BS/MS degree Biology or Related
Experience: 1 year minimum experience

Biotechnology Regenerative Laboratory Research Technician Aseptic Cellular Tissue culture Biology Immunology Apoptosis Immunofluorescence


Contact:
Lisa Conley
Job Type:Employee
Job Status:Full Time
Locations:Pennsylvania-Pittsburgh

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:23 UTCResearch Associate-Process Chemistry
Research Associate wanted immediately to participate in a multi-displinary environment within the Process Chemistry group. The successful candiate is expected to contribute to the rapid development of scalable process and and synthesize and purify target molecules to support pre-clinical programs. He or she will also participate in designing, evaluating, and optimizing synthetic routs for further scale up.
Required skills:

B.S. or M.S. in synthetic organic chemistry with 3-5 years of experience in process research within the pharmaceutical industry
Process chemistry and scale up techniques
Knowledge of synthetic chemistry, purifications, and analytical techniques (HPLC, GC, MS)
Strong written, oral, organizational, and interpersional skill desired.
Must be able to demonstrate a high level of enthusiasm, integrity, and self motivation.
Contact:
Lisa Kwan at Lisa.kwan@labsupport.com
Job Type:Employee
Job Status:Full Time
Locations:Multiple Locations
California-San Francisco
California-Silicon Valley/Peninsula

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:23 UTCResearch Assistant
Job Description:

The purification group in Discovery Chemistry is looking for a motivated individual to assist the team in the many sample handling operations that are involved in the purification of small molecules for Discovery Chemistry. The successful candidate will contribute to the effort by preparing samples for lyophilization, transferring lyophilized samples into vials and using automation instruments to weigh samples and record information in our data system. This person would be responsible for preparing samples and running an analytical LC/MS as well as some purification work as needed. Other work in support of the purification effort may include some roto-evaporation, refilling solvent reservoirs and general maintenance of equipment as needed.
Required skills:

Able to work in a team environment. Previous Lab experience. Must have good communication skills, well organized and some experience with computers or some automation.
Education:
BS in Chemisty is prefered.
Contact:
Lisa Kwan, Lisa.Kwan@labsupport.com and include "Research Assistant" in the subject line.
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:California-San Francisco

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:23 UTCResearch Assistant
Job Description:
A temporary research assistant is needed to support projects in Research and early Development. S/he will develop and implement protein binding assays including ELISAs and cell-based bioassays for protein/antibody quantification and characterization. S/he will work collaboratively with members of Research and Development Sciences. The candidate will handle biohazardous materials, and must adhere to corporate safety standards in all aspects of the work. S/he will use automated liquid handling and robotic systems, and will analyze data and report results using specialized software in multiple assay methodologies.
Required skills:

A minimum of 3 years related work experience is required. Experience with immunoassay development and cell culture is key; additional experience with assay multiplexing, FACS, molecular biology, or automation is a plus. The candidate must be able to apply analytical skills and judgment in assessing the quality of assay data and performance, must be self-motivated, detail oriented, and able to multi-task to meet timelines efficiently and productively. We are seeking a highly motivated candidate who possesses strong analytical skills, excellent verbal and written interpersonal communication skills, ability to keep detailed and accurate records, and the capacity and desire to learn a variety of assay-related methodologies.
Education:
B.S. degree with at least 3 years lab experience.
Contact:
Lisa Kwan, Lisa.Kwan@labsupport.com and include "Research Assistant" in the subject line.
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:California-San Francisco

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:23 UTCResearch Associate
Job Description:

We are seeking a temporary research associate to join our protein purification team within the Protein Chemistry department. The candidate will perform purification of recombinant proteins for research projects using standard purification techniques such as affinity, ion-exchange, hydrophobic interaction, and size exclusion chromatography. In addition to performing protein purifications, the candidate will be responsible for protein characterization using mass spectrometry, laser light scattering, SDS-PAGE, western blots, and other standard biochemical/biophysical methods. The successful candidate should have strong written and oral communication skills, be able to rapidly learn new skill sets and techniques, and demonstrate the ability to work well in a team-oriented environment.
Required skills:

Experience with affinity chromatography methods (including Protein A, IMAC, and anti-FLAG) and secondary purification methods (IEX, HIC, and SEC) along with a working knowledge of AKTA FPLC purification systems and Unicorn software are required. In addition, familiarity with protein characterization methods such as LC/MS and SEC-MALS are desired. Experience with heterologous protein expression in E. coli and mammalian cell culture is a plus.
Strong organizational, communication, problem solving and interpersonal skills are required. The candidate must be team-oriented, dependable, and a self-starter. Ability to follow detailed verbal and written instruction and communicate effectively with scientists is essential. Must be self-motivated, able to multi-task, and meet timelines efficiently and productively.
Education:
BA/BS or MS in Biochemistry or equivalent experience in protein purification
Contact:
Lisa Kwan, Lisa.Kwan@labsupport.com and include "Research Associate" in the subject line.
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:California-San Francisco

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:23 UTCResearch Associate
Job Description:
We are seeking an experienced temporary Research Associate/Senior Research Associate in Antibody Engineering Department at Genentech. Our group focuses on molecular hybridoma cloning and collaborates with diverse discovery biology areas in Genentech.
Required skills:

The candidate must have excellent molecular biology skills such as RNA isolation, cloning, PCR, RT-PCR, 5’-RACE, sequencing and data analysis. Preference will be given to candidates who also have experience in hybridoma cloning, automation, Elisa, Biacore, and Octet. The candidate must demonstrate outstanding communication and problem-solving skills. The candidate is expected to be flexible, creative, and able to master new techniques as needed.
Education:
The successful applicant must have a B.S/M.S in Molecular Biology, Biochemistry, Cell Biology or a related discipline with a minimum of 3+ years of industry and/or academic experience is required.
Contact:
Lisa Kwan, Lisa.Kwan@labsupport.com and include "Research Associate" in the subject line.
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:California-San Francisco

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:23 UTCResearch Associate
Job Description:
Perform antibody, cell-based and other immunoassays as well as PCR based assay to support research projects.
Required skills:

ELISA, PCR, mammalian cell culture, sterile technique, protein assay, Excel, Powerpoint and Word compute applications
Education:
BS in biochemistry or related field and relevant laboratory experience
Contact:
Lisa Kwan, Lisa.Kwan@labsupport.com and include "Research Associate" in the subject line.
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:California-San Francisco

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:23 UTCResearch Associate
Job Description:
We are seeking an experienced research associate to represent the Protein Chemistry department on therapeutic antibody project teams. The successful candidate is expected to work independently and display professional judgment in all aspects of daily research and presentations. The candidate will work with project teams to validate therapeutic targets and generate therapeutic bivalent and bispecific antibodies against those targets. The candidate should be team-oriented, hard-working, friendly and interested in learning new skills.
Required skills:

This position requires a detailed knowledge of biochemistry and antibody engineering and will make extensive use of protein purification techniques including affinity, ion exchange, size exclusion (SEC), hydrophobic interaction and reverse phase chromatography using HPLC and FPLC platforms. Detailed knowledge of protein characterization by techniques such as mass spectroscopy (LC/MS), SEC / Laser Light Scattering (MALLS), SDS-PAGE, ELISA and immunoblot assays, as well as determination of ligand binding constants and enzyme kinetics using surface plasmon resonance (SPR), fluorogenic reagents and ligand assays is essential. Knowledge of related techniques such as sub-cloning, protein expression in mammalian cells, E. coli expression and refolding and mammalian cell culture and cell sorting will be helpful.
Education:
M.S. or Ph.D. in Biochemistry, Chemistry, Molecular Biology or a related field.
Contact:
Lisa Kwan, Lisa.Kwan@labsupport.com and include "Research Associate" in the subject line.
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:California-San Francisco

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:23 UTCResearch Associate
Job Description:
A temp position is open immediately in research discovery. The candidate will support research projects in the area of immunological diseases. Responsibilities will include developing and performing immunoassays (ELISAs) and cell-based bioassays for the screening and characterization of large molecule drug candidates. The candidate will handle biohazardous and cytotoxic materials, and will adhere to corporate safety standards in all aspects of the work. S/he will use automated liquid handling systems and robotic systems, and will analyze data and report results using specialized software for multiple assay methodologies.
Required skills:

Demonstrated skill with cell culture and quantitative immunoassays (ELISAs) are required; experience with using quantitative ELISAs to support PK/PD and efficacy studies is a plus. S/he will be able to apply analytical skills and judgment in assessing assay performance and the quality of assay data.
Must be self-motivated, detail oriented, and able to multitask and meet timelines efficiently and productively. Strong verbal and written communication skills, listening skills, and interpersonal skills are required.
Education:
B.S. or M.S. degree with at least 5 years lab experience.
Contact:
Lisa Kwan, Lisa.Kwan@labsupport.com and include "Research Associate" in the subject line.
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:California-San Francisco

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:23 UTCResearch Associate
Job Description:
A temp position is open immediately in research discovery. The candidate will support research projects in the area of immunological diseases. Responsibilities will include developing and performing immunoassays (ELISAs) and cell-based bioassays for screening and characterizing large molecule drug candidates. The candidate will handle biohazardous, and cytotoxic materials, and adhere to corporate safety standards in all aspects of the work. S/he will use automated liquid handling systems and robotic systems, and will analyze data and report results using specialized software in multiple assay methodologies.
Required skills:

Skills and experience with quantitative ELISAs and cell culture are required. Previous experience with quantitative ELISA to support PK/PD, efficacy studies is a plus. S/he will be able to apply analytical skills and judgment in assessing the quality of assay data and assay performance. Must be self-motivated, able to multi-task, and meet timelines efficiently and productively. Strong verbal communication, writing, and listening skills, as well as interpersonal skills required.
Education:
B.S. degree with at least 3 years lab experience
Contact:
Lisa Kwan, Lisa.Kwan@labsupport.com and include "Research Associate" in the subject line.
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:California-San Francisco

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:23 UTCManufacturing Technician
Job Description:
******Positions for all shifts available*******
Responsible for producing innovative biotherapeutic medicine by interfacing with highly automated production systems and controls in cGMP manufacturing environment, and maintain areas in high state of inspection preparedness. Operates production equipment for cell culture that may include culture growth, process monitoring, sampling, harvesting, and transfer. Performs media/buffer solution preparation operations. Maintains records and clean room environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP).
Responsible for being proficient in one functional area. Understands and applies biological, chemical and mechanical principles and techniques.
Required skills:


Must possess good problem solving, interpersonal communication, and team skills. Must be a self-starter with a strong focus on quality, details, and results. Must be able to work weekends, off-shifts, and overtime as required. Mechanical aptitude and a familiarity with computer based systems is preferred. Must be able to lift 40 pounds and stand for extended periods of time.
Education:

A high school degree with some college-level course work in biological sciences, physical sciences, or engineering with at least 2 years of relevant biopharmaceutical experience.
Contact:
Marilyn Rosa, Marilyn.Rosa@labsupport.com and include "Manufacturing Technician" in the subject line.
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:California-San Francisco

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:23 UTCQc Analyst I
Job Description:
Responsible for support activities for Small Molecule Analytical and Quality Control Laboratories, which may include, but are not limited to, the following:
Coordinate vendor maintenance qualifications, create repetitive maintenance plans, and/or create bill of materials for vendor parts in SAP.Coordinate with system owners, vendors, Facilities & Quality to plan & schedule PM & repairs for SMACQC lab equipment. Obtain pre-approval Signatures from Quality/System Owner for Non-Agilent and Non-Waters systems when a qualification will be performed. Review vendors' documents after maintenance/repair work are completed using cGMPs and complete an entry in maintenance logbook. Provide support for continuous improvement projects for Facilities, Quality, and Small Molecule QC Lab. Provide support document filing and archival.
Order chemicals and supplies. Perform small equipment maintenance and calibration (pipettes) and various administrative support duties.
Maintain temperature monitoring units and assist in routine sweeps of the lab to ensure compliance with cGMP. Schedule and/or coordinate equipment maintenance, and perform periodic review. Maintain housekeeping in the SMACQC labs.
Support SMACQC with data scanning and archival. Apply significant knowledge of compliance requirements to maintain an inspection ready state.Accomplish corporate, operational and departmental goals. Maintain and archive GMP equipment logbook documentation. Assist with SMACQC process improvements.
Required skills:

Experience/awareness in Quality Control is highly desired. Familiarity with basic analytical laboratory equipment, such as balances, pH meters, spectrophotometers and SAP software is a plus.
Education:
Bachelor Degree preferred (Associates Degree acceptable) in Physical/Biological Science.
Contact:
Marilyn Rosa, Marilyn.Rosa@labsupport.com and include "Qc Analyst I" in the subject line.
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:California-San Francisco

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:23 UTCResearch Associate
Job Description:
The Late Stage Pharmaceutical Development department at Genentech has an open temporary position for a Research Assistant/Research Associate in the Commercial Product Support group. The position icludes providing analytical support for engineering and development studies to support manufacturing transfers, investigations, and discrepecies for Marketed Products. The successful candidate will have strong multi-tasking and documentation skills and should be comfortable working both independently with minimal supervision and as part of a team.
Required skills:

Lab experience including the ability to characterize proteins with multiple HPLC techniques (SEC, IEC, RPLC, etc.) and electrophoretic methods (CE-SDS) is preferred. Must possess strong organizational, verbal communication, writing, listening, and interpersonal skills. Able to meet timelines both efficiently and productively with the ability to follow detailed verbal and written instruction. Must be self-motivated and able to multi-task. Familiarity with cGMP preferred.
Education:
A BA/BS/MS in Pharmaceutical Sciences, Biology, Chemistry, Chemical Engineering, Biochemistry, Biophysics, or related fields with 2 - 5 years of relevant laboratory experience is required.
Contact:
Marilyn Rosa, Marilyn.Rosa@labsupport.com and include "Research Associate" in the subject line.
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:California-San Francisco

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:23 UTCSample Handling Technician
Job Description:
Participates to all CSO activities related to sample handling, as assigned by the CSO Laboratory Head and/or Senior Sample Handling Technician.
Provides administrative support to CSO site, as appropriate.
Carries out all sample handling activities according to local health and safety rules and applicable SOPs.
Provides assistance to the CSO Laboratory Head and Senior Sample Handling Technician and reviews shipments dates to ensure that the samples are handled and that the shipments are organised within the agreed timelines.
Liaises with customers, as appropriate, to provide status updates on study related activities.
Coordinates and tracks sample shipments sent to CSO.
Packs out and checks received samples.
Logs samples into the sample management database.
Ensures samples are stored according to requirements
Handling of sample discrepancies
Prepares and packs samples for dispatch according to the applicable transport regulations.
Organizes and tracks sample shipments to analytical laboratories or sites.
Arranges for transport material and boxes/dry ice, as requested.
Checks and updates stocks regarding commonly used material for sample handling and sample shipments, as appropriate.
Liaises with Roche Couriers or Roche shipping department when appropriate.
Completes files and archives all relevant study documentation according to the applicable SOPs.
Coordinates efforts with other CSO staff on study related issues.
Provides CSO Laboratory Head with regular input on local CSO issues and practices related to sample handling and shipment tracking activities, and collates information as appropriate.
Provides CSO Laboratory Head with regular input on health and safety issues, and collates information as appropriate.
Writes and reviews local and global CSO SOPs and supports the CSO Laboratory Head in
Implementing new CSO systems and SOPs.
Ensures that the sample management database is maintained up to date and is in accordance with the completed study activities.
Required skills:

Demonstrates familiarity with computer technology.
Good communication (written and verbal) skills in English.
Ability to resist stress and time pressure
Good organizational skills
Focus on value & Customer, Align for Success, Learn for the Future
Education:
Minimum: Associates Degree or equivalent recognized qualification.
Contact:
Marilyn Rosa, Marilyn.Rosa@labsupport.com and include "Sample Handling Technician" in the subject line.
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:California-San Francisco

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:23 UTCSenior Technical Manager
Job Description:
Author or revise Quality Agreements supporting collaborations within Roche.
Author or revise Product Specific Requirement documents supporting collaborations within Roche.
Serve as project coordinator for process improvement initiatives.
Compile and report out monthly data for Quality Issues at Contract Manufacturing sites.
Prepare documentation for batch record review process and collaborate with Site Manager to complete batch assessments.
Data entry in Development database.
Data archival
Required skills:

Provide review for Depot batch records.
Provide assistance to Partners and Depots regarding quality inquiries.
Establish work priorities to meet targets and timelines.
Complete Destruction processing
Gather all required documentation to support QP release activities at CMOs.
Sound knowledge of cGMPs or equivalent regulations
Ability to interpret and relate Quality standards for implementation and review
Ability to make sound decisions about scheduling, allocation of resources, and managing priorities
Ability to communicate clearly and professionally both in writing and verbally
Flexibility in problem solving, providing direction and work hours to meet business objectives
Excellent written and verbal communication skills
Strong interpersonal skills
Education:
University degree, preferably in Life Sciences.
Proven knowledge of GMPs, health authority regulations, and other international standards
Demonstrated knowledge and execution of Quality operations and processes
At least 3 years working experience in quality with experience in quality function in packaging operations
Contact:
Marilyn Rosa, Marilyn.Rosa@labsupport.com and include "Senior Technical Manager" in the subject line.
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:California-San Francisco

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:23 UTCTechnical Writer II
Job Description:
Manufacturing Technical Writer
The main purpose of this position is to revise the written content of Batch Production Records and SOP’s to be used by manufacturing associates. This is a full-time temporary contract (6-12 months) with a possibility of an extension.
JOB DUTIES:
Create new or revise existing content for SOPs and BPDs with a high degree of quality in accordance with cGMP requirements and corporate guidelines
Work collaboratively with project team members including Manufacturing, Engineering, Process Development, Quality and other subject-matter experts to solidify content.
Participate in project team meetings.
Other related duties that may be called upon.
Required skills:

Experience in a Quality Control environment; knowledge of GMP and/or ISO standards.
Experience in biotech and/or pharmaceutical manufacturing environment an asset.
Minimum two (2) to five (5) years related experience in technical writing.
Detail oriented with the ability to learn new concepts and apply them quickly.
Good command of MS Office Suite (Word, Excel, PowerPoint, Outlook)
Exceptional written and verbal English communication skills.
Strong working knowledge of editing, proofreading, spelling, grammar, and punctuation.
Skilled at organizing information into a clear, concise written form.
Ability to multi-task and to work in a deadline-driven environment.
Able to work independently as well as in a team environment.
Education:
Bachelor Degree in Science preferred
Contact:
Marilyn Rosa, marilyn.rosa@labsupport.com and include "Technical Writer II" in the subject line.
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:California-Oakland/East Bay

Categories:Pharmaceutical]]>Thu, 23 May 2013 10:28:23 UTCAnalytical Research & Development Scientist

We are presently recruiting for an experienced Analytical Chemist to join a tenured department and provide expert support of instrumental and USP testing methods. This role will be responsible for:
Wet chemistry and instrumental analysis using techniques such as HPLC/UPLC, UV/V1S, IR, GC and dissolution methods.
Istrumental analysis using UV/Vis, FTIR, Dissolution; more complex analyses using HPLC; GC, robotics systems and more complex wet chemistry tests on pharmaceutical samples (viscosity & titration), using LIMS where required
Operation of lab equipment, preparation of reagents for testing and data analysis activities.
Accurate records in lab notebooks of all testing performed.
Instrumental troubleshooting and routine maintenance
Regulatory compliance with all SOP's and applicable regulatory requirements.
Adhere to all established safety procedures and ensure a safe work area.
Data analysis of chromatographic results





Required skills:

This successful candidate will possess the following qualifications:
BS/MS degree in Chemistry, Pharmaceutical Sciences or related discipline
Pharmaceutical industry experience (3+ years)
Solid working and theoretical knowledge of HPLC, UV, IR, GC, dissolution testing and wet chemistry methods
Knowledge and understanding of USP, cGMP and FDA regulations
Excellent written and verbal communication skills.
Technical writing, notebook documentation and report writing skills
Demonstrated ability to work in a team environment and communicate effectively with team members, external customers and management personnel as necessary
Ability to work independently with limited supervision
Proficient in MS Office applications (Word, Excel, Outlook...)
Contact:
Marshena Moncrieffe (914) 683-5700
Job Type:Employee
Job Status:Full Time
Locations:Multiple Locations
New Jersey-Northern
New York-Albany/Poughkeepsie
New York-Westchester

Categories:Pharmaceutical]]>Thu, 23 May 2013 10:28:23 UTCAnimal Research Associate
This position is for a Research Associate in the Breeding team. The breeding team is responsible for the breeding and maintenance of several transgenic mouse models for various research groups. Primary tasks performed on a daily basis in mice include:
Setting up breedings, checking for plugs, identifying neonates, ear notching, toe tattooing, tail tattooing, ear tagging, weaning, sacrificing animals and identifying/treating common mouse health issues. Other tasks such as adult dosing and sentinel blood collection/processing may be required.
Ideal candidate must be able to account for every mouse in the colony and maintain clear and accurate files. Must be proficient at using Microsoft Excel and Word. Strong organizational and multitasking skills required. Must review, comprehend and comply with all SOPs and IACUC, safety and quality assurance standards related to assigned work area at all times..

Required skills:

Animal technician with at least 2 years of mice handling and breeding experience. Leadership, organizational, multi-tasking skills required along with willingness and ability to work independently and as part of a team. Occasional weekend work required.
Contact:
Marshena Moncrieffe 914-683-5700
Job Type:Employee
Job Status:Full Time
Locations:Multiple Locations
New York-New York City
New York-Westchester

Categories:Multiple Categories
Biotechnology
Pharmaceutical]]>Thu, 23 May 2013 10:28:23 UTCQA Associate
Perform batch record review concurrent to completion of manufacturing operations in real time.
Perform routine quality audits in Manufacturing.
Support quality systems related to QA for in-process sampling and controls, and all aspects of shop floor QA.
Act as quality representative on the floor during manufacturing areas.
Support the development of SOPs and batch records.
Required skills:

Experience in QA operations on manufacturing floor, batch record review and approval.
Knowledge of regulatory requirements for pharmaceutical, biotech and vaccine industries.
Experience in fill/finish operations.
Experience in writing deviations and investigations, and using enterprise systems.
Minimum 5 years QA experience.
Education:
BS in the biological sciences, engineering or biotech.

**This is position requires frequent 3pm - 11pm shift coverage. The employee will primarily work M-F, 8am - 5pm, but must have the ability to cover 3pm - 11pm for weeks at a time **
Contact:
Natalie Maghen natalie.maghen@labsupport.com
Job Type:Contract Hire
Job Status:Full Time
Locations:North Carolina-Holly Springs

Categories:Pharmaceutical]]>Thu, 23 May 2013 10:28:23 UTCng complex data into technical reports; follow GMP and QSR compliance guidance.




Required skills:

Handling DNA and blood samples; PCR; ELISA; serology; DNA sequencing; and/ or genotyping; analytical, detail oriented, great follow through, interpersonal relationships; takes initiative, resourceful, independent.

Education:
Minimum Bachelor’s Degree in Molecular Biology, Biochemistry, Immunology. Three years of lab experience preferred.

Contact:
Natalie Maghen natalie.maghen@labsupport.com
Job Type:Contract Hire
Job Status:Full Time
Locations:Wisconsin-Milwaukee

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:23 UTCFood Safety Coordinator
A Leader in the Food and Beverage industry is seeking a Food Safety Coordinator on a Direct Hire basis due to growth. This is a newly created position reporting to the QA Manager. The Food Safety Coordinator has the responsibility for the coordination, execution and implementation of key microbiology and food safety programs for the site, which includes HACCP plan development and validation, Pathogen Environmental Monitoring, Sanitation and other food safety initiatives and certifications.
Job Description :
1. Provide scientific and technical food safety and microbiological support to the site to ensure product safety and quality, through risk assessment, program development and training.
2. Coordinates, plans, and implements quality, food safety, and sanitation programs for the facility.
3. Identify and communicate food safety risks to site, giving actionable advice on Food Safety programs and incorporating into programs
4. Conduct validation of Critical Control Points related to heat kill steps (Cooking, roasting, etc) and assess validity of data.
5. Conduct validation studies and risk assessments to determine critical limits for critical processes and collaborate with internal and external resources to update/maintain procedures.
Required skills:

Requirements
1. Position requires a B.S. in a food safety discipline (Microbiology, Food Safety, Food Science or related field) with a minimum 2 years experience in Quality and/or Food Safety including experience in food industry auditing. GFSI practitioner or certified auditor preferred.
2. Previous HACCP certification program design and implementation is required.
3. Thorough technical knowledge of quality & food safety is required.
4. Strong written & verbal communication skills, analytical ability, leadership strengths and ability to work effectively with a team are required.
5. Computer software skills to include Word, Excel and PowerPoint required.
6. Knowledge of HACCP, GMP, Pathogen Environmental Monitoring and Facility/Equipment Design
Contact:
Philadelphia Lab Support at 610-660-9830
Job Type:Employee
Job Status:Full Time
Locations:Multiple Locations
New Jersey-Southern
Pennsylvania-Harrisburg
Pennsylvania-Philadelphia

Categories:Food & Beverage]]>Thu, 23 May 2013 10:28:22 UTCFood QA Coordinator
A Leader in the Food and Beverage industry is seeking a Food QA Coordinator on a Direct Hire basis due to growth. This is a newly created position reporting to the QA Supervisor. The QA Coordinator has the responsibility to coordinate activities of technicians, maintain quality assurance programs as per Policies and Procedures. The Lab Coordinator must be able to communicate and interact with appropriate personnel pertinent information and data as required. The Coordinator must possess the ability to manage and coordinate multiple activities as well as urgent requests in a professional and timely manner. Excellent understanding of principles of Food Safety, Laboratory Safety and Quality Assurance with ability to train fellow employees and facilitate plant wide programs.


Required skills:


·BA/BS degree (Food Science, Microbiology, Biology, preferred).
·High Level of Computer Competency ( SAP, Microsoft Office)
·Excellent written and oral communication skills.
·High Level of experience in the Food Industry or related GMP regulated industry highly desirable.
-Understanding of Food Safety, HACCP, and GMP principles highly desirable.
-Exposure to and experience with ISO, GFSI (BRC/SQF), Kosher, Regulatory highly desirable.
Contact:
Philadelphia Lab Support at 610-660-9830
Job Type:Employee
Job Status:Full Time
Locations:Multiple Locations
New Jersey-Southern
Pennsylvania-Harrisburg
Pennsylvania-Philadelphia

Categories:Food & Beverage]]>Thu, 23 May 2013 10:28:22 UTCLab Research Chemist
Lab Research Chemist Opportunity available in Maplewood, MN. This is initially a 12-month contract, full-time position.
Description
· Initiate and complete technical activities leading to new or improved products or processes which have significant impact potential at a program level
· Establish and cultivate a network of support (laboratory, manufacturing, engineering sales and marketing) to facilitate completion of assignments.
· Participate in project planning, and documents experimental data/observations in technical notebooks (or approved electronic files), prepares reports, and makes oral presentations.

Required skills:

Equipment & Knowledge
· GC (Gas Chromatography) and HPLC (High Performance Liquid Chromatography)
· Sound knowledge of chemistry fundamentals, laboratory skills in chemistry including sample preparation.

Good written and oral communications skills are essential for communicating with problem solving teams and for documenting results.

Education:
BS degree in Chemistry or related field




Core Hours – Monday – Friday

Contact:
Please apply with your most up-to-date resume (Reference #15961) Brittany.Yarbrow@labsupport.com
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:Multiple Locations
Minnesota-Maplewood
Minnesota-Minneapolis
Minnesota-St. Paul

Categories:Multiple Categories
Biotechnology
Chemical Industry
Environmental Services
Food & Beverage
Materials Science
Medical Device
Pharmaceutical]]>Thu, 23 May 2013 10:28:22 UTCChemist III / Technical Writer
Pharmaceutical Company in North Chicago is seeking a Chemist III / Technical Writer for initially an 8-month contract, full-time position.

Description:
Completing multiple documentation-related activities including: writing method validation protocols and reports, verification of laboratory records, preparation of data summaries, and entering information into databases.

Required skills:

· Must have proven experience with good technical writing skills and attention to detail
· BS in Chemistry 7+ years experience OR MS in Chemistry 2+ years experience.
· Must have experience with Microsoft Word, Excel, ChemDraw, and databases
· Working knowledge of instruments, strong lab skills.
· Strong documentation skills, strong GMP, GLP.
· May have publications, or experience in presentation of findings to scientific organizations


Contact:
Please apply with your most up-to-date resume (Reference #2343) Brittany.Yarbrow@labsupport.com
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:Multiple Locations
Illinois-Lake County
Illinois-Chicago North

Categories:Multiple Categories
Biotechnology
Chemical Industry
Medical Writing (Regulatory & Publications)
Pharmaceutical
Quality Assurance]]>Thu, 23 May 2013 10:28:12 UTCAssociate Scientist II
A Global Life Sciences Company is seeking an Associate Scientist II in South San Francisco, CA for initially a 6-month contract full-time position
Description: Prepare Ion sequencing sample, perform template amplification, sample enrichments, sequencing and data analysis and generating detailed concise technical reports
Duties:
· Conduct routine scientific experiments using common laboratory equipment and calculations.
· Assist or on occasion drive the evaluation and procurement of equipment and materials.
· Make detailed observations and analyze data.
· Maintain accurate lab notebook and training file in accordance with Division standard.
· Assist supervisor in the interpretation of experiment results, including factors that may affect quality, accuracy, timeliness and usefulness of data.
· Suggest options for additional experiments and troubleshoot experiments.
· Plan well understood technical options to reach a specific technical objective. Identify and solve elementary problems in experimental designs.
· Contribute ideas and suggestions to improve standard laboratory techniques, improve protocols, processes and equipment.
· Lead the documentation of repeatable lab procedures as required.
· Read literature directly associated with assigned project.
· Maintain some familiarity with competitive products and assist with competitive audits or documentation as required.
· Comply with all company safety regulations and procedures.
· Report non-compliance and may serve as team lead.
· Suggest improvements in safety and productivity based on solid technical understanding of expected R&D outcomes.
Required skills:

Knowledge and familiarity of:
· PCR and RPA amplification methods
· Ion library preparation methods
· Ion sequencing platforms, including PGMs and Protons
· Ion sequencing data analysis pipeline.
· Understanding of the New Product Introduction process and impacts business opportunities through successful task completion
Education: Requires a PhD in Biology, Chemistry, Biochemistry, or other related discipline, or the equivalent knowledge and experience with 5 years of industry experience



Contact:
Please apply with your most up-to-date resume (Reference #236) Brittany.Yarbrow@labsupport.com
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:Multiple Locations
California-South San Francisco
California-San Francisco

Categories:Multiple Categories
Biotechnology
Quality Assurance]]>Thu, 23 May 2013 10:28:12 UTCProduction Scientist
Biomedical Manufacturing company is seeking a Production Scientist in Chaska, MN for initially a 2-month contract position, expected to extend to 6 months (end of 2013).

Job Duties and Responsibilities:
Performs simple calculations according to procedures, and maintains accurate records of work performed according to GLP, GMP, and QSRs
Manufactures buffers and diluents according to standard operating procedures and work instructions
Participates on a Continuous Process Improvement Team, and is a contributor to team efforts within the department
Typically receives minimal instruction on routine work; general instruction son new assignments Follows standard practices and procedures in analyzing situations or data from which answers can be readily obtained
Required skills:

Bachelor’s Degree in Biological Sciences, Chemistry or related field required
Previous laboratory work experience preferred, especially in an FDA/ISO regulated manufacturing environment
Must be able to follow approved work instructions with attention to detail
Ability to prioritize work tasks
Ability to work within a team environment
Possesses excellent communication and time management skills
Experience with MS Office products, email
Contact:
Please apply with your most up-to-date resume (Reference #9698) Brittany.Yarbrow@labsupport.com
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:Multiple Locations
Minnesota-Chaska
Minnesota-Minneapolis

Categories:Multiple Categories
Biotechnology
Chemical Industry
Medical Device]]>Thu, 23 May 2013 10:28:12 UTCSr. Scientist
Seeking a Sr. Scientist/Medical Technologist in Des Plaines, IL for initially a 1-year contract, full-time position.

Description:
Medical Technology and Software background
Required skills:

· Experienced/skilled in use of Fluorescent In-Situ Hybridization (FISH) with concentration in blood.
· Must have experience with Molecular Biology
· Bachelors in either Biology or Biochemistry.
· Must be very familiar with all Cell Dyn systems to set up the systems, collect data and analyze the collected data.
· Must also be familiar with blood cell morphology to be able to collect reference data.
· Must be able to conduct experiments with minimum supervision to develop CDX Cal/Con.
· Must be able to analyze RBC Morphology data using the 3D surface analysis software program (software knowledge in addition to medical technology and Cell Dyn systems knowledge required).
· Must have a good understanding in clinical applications of Cell Dyn methods

Contact:
Please apply with your most up-yo-date resume (Reference #43528) Brittany.Yarbrow@labsupport.com
Job Type:Temporary
Contract
Project
Job Status:Full Time
Locations:Multiple Locations
Illinois-Des Plaines
Illinois-Chicago
Illinois-Chicago North
Illinois-Chicago South

Categories:Multiple Categories
Biotechnology
Clinical Data Management
Scientist/Specialist]]>Thu, 23 May 2013 10:28:12 UTCResearch Associate

We are seeking an experienced Development Research Associate. The candidate should have extensive experience in mammalian cell culture, with primary cells and transfection. In addition, the position will require someone with experience in RNA and genomic DNA purification, Real-time PCR, Western blot, and cloning. The candidate must possess strong written and oral communication skills, and is dedicated to support and achieve team project goals.

Required skills:

Bachelors or Masters in Molecular & Cell Biology or equivalent discipline
5+ years related experience
**Please email your resume to jasmine.shu@labsupport.com and use "RA-Drug Discovery" as the subject line.
Contact:
Please email your resume to: jasmine.shu@labsupport.com
Job Type:Contract Hire
Job Status:Full Time
Locations:California-Oakland/East Bay

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:12 UTCManufacturing Technician - BioProcess
MUST BE ABLE TO WORK ANY SHIFT AT ANY GIVEN TIME-FLEXIBILITY IN SCHEDULE IS HIGHLY IMPORTANT TO OUR CLIENT.
Responsibilities:
• Adhere to all plant safety policies and procedures and proactively identify unsafe conditions.
• Perform safety and housekeeping audits as required.
• Assist in, set up, change over, and test run equipment for various-sized vials and packages as required.
• Supporting the Operations Specialist, Maintenance, and/or outside services in the repair, maintenance, and calibration of Genentech systems as required.
• Perform training of other Technicians.
• Assist in the development of plant SOPs and training materials.
• Execute production recipes, check-in equipment, and perform material movements using automated computer software applications (SAP and MES systems).
• Operate all formulation, sterile filling, inspection, and final vial packaging equipment in the plant.
• Perform material handling in the plant as required.
• Perform preparation of sterile components.
• Assist in the cleaning, set-up, sterilization, and disassembly on a variety of processing equipment.
• Perform bulk thaw, dilution, and formulation operations.
• Perform manual inspection of empty vials and filled product with a focus on quality and efficiency.
• Conduct environmental monitoring activities in the manufacturing areas as required.
• Prior to start-up, during processing, and at the completion of the manufacturing process, perform all documentation and clerical functions to provide the proper accountability and traceability of components and finished product.
• At the start and finish of each shift, report and make recommendations regarding equipment, supplies, and required repairs.
• Process concerns, safety concerns, and areas for improvement in reliability, yield, and efficiency.
• Work effectively and efficiently in a team-oriented environment to ensure maximum and high-quality output.
• Perform cleaning and housekeeping duties as required.

Required skills:

MUST BE ABLE TO WORK ANY SHIFT AT ANY GIVEN TIME-FLEXIBILITY IN SCHEDULE IS HIGHLY IMPORTANT TO OUR CLIENT.
Proficiency in the English language—reading, writing, and communication.
• Must be able to work all shifts (1st, 2nd, or 3rd), put in required overtime as needed, be able to lift 45 pounds, and stand for extended periods of time.
• In addition, all candidates must pass a vision acuity and color discrimination test.
• Must complete periodic physical examinations to identify medical conditions that pose a risk to Grade C or higher operation.
• One to two years (within the last seven years) experience in the operation of complex mechanical equipment used in the washing, filling, conveying, sealing, inspection and packaging of products/containers is highly desirable. Target industries include pharmaceutical, biotechnology, biomedical, electronic, chemical, food, cosmetics, and/or other medical industries.


Contact:
portland@labsupport.com
Job Type:Contract Hire
Job Status:Full Time
Locations:Oregon-Portland

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:12 UTCLaboratory Technician
Lab Support is currently seeking a full-time lab technician to work within our client's Quality Assurance departments. Duties include microbiological, chemical and physical testing of incoming raw materials, work in process and finished goods. Candidate will be required to obtain and maintain licenses for certification, if hired. Multiple shift requirements needed and candidate must be willing to work weekends and holidays.

Required skills:

Qualified candidates must have an Associates degree in Science with basic chemistry and microbiology or 2 years previous lab experience, strong math, communication and computer skills. Previous food testing background or dairy experience preferred. Knowledge of GMP’s and SPC plating a plus.
Contact:
Rena Venturini
Job Type:Contract Hire
Job Status:Full Time
Locations:Multiple Locations
New York-Buffalo
Pennsylvania-Pittsburgh

Categories:Food & Beverage]]>Thu, 23 May 2013 10:28:12 UTCLab Technologist
Our client, a growing Health Services company located in Richmond, VA is seeking qualified candidates for a Lab Technologist opportunity. Position requires performing routine moderate to complex laboratory techniques within a Molecular/Genetics laboratory.
Prior Medical Technologist/ Lab Technologist experience is required
Prior experience working in Molecular/Genetics Lab
Ideal candidates able to work 2nd or 3rd shift
Required skills:

BS in Biochemistry or Forensics, or similar discipline
Min 3-5 years experiences in Molecular or Genetics lab

Contact:
Rockville Lab Support
Job Type:Employee
Job Status:Full Time
Locations:Virginia-Richmond

Categories:Biotechnology]]>Thu, 23 May 2013 10:28:12 UTCQC Analyst
Our client, a leading alternative energy researcher, is seeking a QC Analyst to be responsible for conducting quality control routine and non-routine analysis of raw materials, in process, and finished formulation enzyme products according to standard operating procedures. Job scope includes performing new method development, method improvements and validation of enzyme activity determination or supporting assays.

Critical Competencies:
· Conducts microbiological and analytical analyses according to standard operating procedures (SOPs)
· Compiles data and records results
· Reviews results for compliance to specifications and reports deviations
· Analyzes data and prepares reports, upon request
· Prepares and revises SOPs and test methods, as required
· Conducts necessary maintenance and calibration of lab equipment
· Conducts problem solving on analytical and instrument issues, as required
· Applies knowledge of good laboratory practices on a daily basis
· Performs method transfer to and training of toll manufacturing personnel

Required skills:





Education/Experience:
BS in Biological Sciences or related field and 1-2 years experience working with enzymes or proteins and running colorimetric enzyme assays preferred. General molecular biology and biochemistry laboratory techniques, including: gel electrophoresis, spectrophotometry, a basic understanding of enzyme-catalyzed reactions and kinetics is required. Any analytical experience such as HPLC would be advantageous. Bilingual in English and Spanish is a plus.

Contact:
sandiego@labsupport.com
Job Type:Employee
Job Status:Full Time
Locations:California-San Diego

Categories:Multiple Categories
Biotechnology
Pharmaceutical]]>Thu, 23 May 2013 10:28:12 UTC