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 Analytical Biochemistry Associate II

Details
Country: USA
Location: Irvine CA
Total applied: 40
Location: US-CA-Irvine
Job Ref Code: 1137~WQG~665931P1~41
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . About Kforce
. . . . . . . . . . . . . With over 40 years of experience, Kforce continues to set the standard in the Clinical Research Staffing industry with an unwavering commitment to provide our candidates with exceptional service in meeting their employment and career needs. Using our nationwide presence, which includes over 1,000 staffing specialists operating in 45 major markets, it's easy to see how we consistently prove that great people really do equal great results.
Kforce is an EEO/AA Employer.
Analytical Biochemistry Associate II

Responsibilities: Kforce is recruiting for an Analytical Biochemistry Associate to work with a biotech company in the Irvine area. The Analytical Biochemistry Associate II is responsible for leading research and development of new and existing methods for characterization of recombinant proteins for human therapeutic use. This individual will take a product through method development and transfer to a quality control department. In addition, this person will assist in training and supporting less experienced analysts. Lab support work such as reagent preparation, record keeping, equipment calibration and qualification, and cGMP documentation may be required. Other duties may include: Perform research and development of new and existing methods for characterization of recombinant proteins. Test recombinant proteins using the following instruments/techniques: UV spectrophotometer, HPLC, Capillary Electrophoresis, SDS-PAGE, FACE Glycosylation Profiling, ELISA, Endotoxin and other related methods. Tabulate and graph data, and prepare technical reports for senior personnel. Perform and transfer analytical methods from AMD to Quality Control (QC) department. Analyze biological material using analytical test methods and SOPs; report results to cross functional teams. Draft and revise GMP documentation to be used by the analytical quality control department such as test methods, formulation methods, and SOPs. Write protocols and reports. Maintain laboratory notebooks and follow GLP and cGMP documentation requirements. Adhere to industry and government standards regarding aseptic technique and safe handling of biohazardous materials. Maintain and calibrate analytical instrumentation when necessary. Troubleshoot instrument failure and report findings. Identify areas for improvement and increased efficiency; assist in implementing approved changes. Comply with all safety policies, practices and procedures. Participate in proactive team efforts to achieve departmental and company goals.If you are not a local candidate but are relocating, please inform me of your arrangements (i.e., date and city/state you are relocating to).Kforce (NASDAQ: KFRC) is a full-service specialty staffing firm providing flexible and permanent staffing solutions for organizations and career management for individuals in the specialty skill areas of information technology, finance & accounting, human resources, engineering, pharmaceutical, health care and scientific. Backed by more than 1,500 recruiting specialists, Kforce operates in more than 40 markets in North America. For more information, please visit our web site at

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