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Job Description Primary responsibility will be to assist in the execution of SOPs and Batch Records in the large scale fermentation/infection and harvest department of cGMP manufacturing facility. Duties will include operation, maintenance, cleaning and sterilization of large6/24/2014 Pearl River, NY Save This Job
Job Summary Applicants should have a M.S. or Ph.D. (Biochemistry, Protein Chemistry, Biotechnology, Biomedical Engg, and Biochemical Engg) with ? 3 years of experience in upstream process development. Proven expertise in recombinant protein expression is essential. A strong6/18/2014 Cambridge, MA Save This Job
Description: FibroGen seeks a Quality Assurance Senior Manager/Associate Director to support the manufacture of Drug Substance and Drug Product at Contract Manufacturing Organizations (CMO) and Contract Research Organizations (CRO) to ensure FibroGen products are in compliance6/30/2014 San Francisco, CA Save This Job
Description: FibroGen seeks a Quality Assurance Associate Director / Director to support the manufacture of Drug Substance and Drug Product at Contract Manufacturing Organizations (CMO) and Contract Research Organizations (CRO) to ensure FibroGen products are in compliance with6/30/2014 San Francisco, CA Save This Job
Reports To: Manager, Quality Assurance Description: Position Overview: This position is responsible for supporting Avid?s quality assurance function for medical imaging drug development (USA and International). Under the direction of the Manager, Quality Assurance, this6/7/2014 Philadelphia, PA Save This Job