QC Analyst 2-3

SUMMARY





The successful candidate will be responsible for routine and non-routine analysis of in process buffers and medias, final products and samples generated from monitoring of the manufacturing processes according to SOPs. This includes performing moderate data analysis and trending, GMP documentation, training of QC personnel and equipment maintenance. Experience in cell based assays, ELISA's, viral assays and/or PCR is desired. Additional responsibilities include transfer new test methods from Assay Development and supervision routine testing. The individual should be knowledgeable in the requirements of a cGMP laboratory and scientific theory and principles. The analyst should be able to work on a variety of problems of diverse scope, perform routine job functions independently and provide guidance to other QC staff.



ESSENTIAL FUNCTIONS





Essential functions include but are not limited to the following:






Carry out routine and non-routine assays following SOPs.


Perform peer review of other QC Analysts' work.


Document results following GMP's as well as write and revise SOP's.


Transfer new test methods, train appropriate staff and initiate routine testing


Must have the ability to work independently as well as on teams.








JOB QUALIFICATIONS (EDUCATION, CERTIFICATIONS, EXPERIENCE)





Bachelor's degree in a scientific discipline or equivalent with 2 to 8 years experience in quality control systems or a Master's degree with 0 to 5 years experience.

OTHER KNOWLEDGE AND SKILLS REQUIRED:





Working knowledge of GMP regulations and their application. Judgment to identify and address problems. Ability to train others in technical assays and the application of GMP. Understanding of basic statistics required in data analysis. Attention to detail, ability to follow procedures rigorously, computer skills and good oral and written communication skills.





CLICK HERE TO APPLY: http://www.cellgenesys.com/job-application.asp?reqno=HW-06-034-N&title=QC+Analyst+2