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Job Summary: The position will provide support for the Quality Assurance group. The candidate will work with cross functional teams to maintain internal quality systems with an emphasis on GCP. Responsibilities: ? Perform routine QA review of Clinical Protocols, Clinical Study8/4/2015 Lexington, MA Save This Job
Job Summary: The candidate will design and perform experiments in order to develop chemical processes for the manufacture drug substances. You will be expected to subsequently undertake the GMP manufacture of these API processes at kilo-lab scale and support manufacture at a CMO8/4/2015 Lexington, MA Save This Job