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Responsible for development, implementation and maintenance of quality assurance systems and activities. Oversees generation and review of documents used in cGMP, monitors audits of production and QC areas, and audits raw material vendors and prepare manufacturing5/16/2015 Mountain View, CA Save This Job
at Blue Apron Blue Apron Headquarters What We Are Looking For: As an innovative, quickly growing company, PR is a very important function at Blue Apron. We?re looking for a seasoned PR professional to lead our PR strategy and ensure we deliver our key messages through every PR6/25/2015 New York, NY Save This Job
NO PHONE CALLS OR AGENCIES PLEASE. In this newly created position, the Program Manager is responsible for the management of all daily program activities for one or more of Company's clinical stage programs. He/she will work closely with functional representatives for assigned6/8/2015 Watertown, MA Save This Job
Reports to: Associate Director Role: The project manager is responsible for reviewing and understanding the scope of the project and the contractual components included (i.e., media materials, advertisements, etc.) and implementing them to meet project enrollment goals as6/19/2015 Horsham, PA Save This Job
Job Location: San Francisco, CA Description: The Drug Safety Associate will be responsible for the review, evaluation and management of adverse event reports from FG-4592, FG-3019, and other clinical trials in accordance with FDA, EMEA, China FDA, other applicable health5/20/2015 San Francisco, CA Save This Job