Required skills Conduct product release using cGMP guidance applied to drug product manufacturing and applicable procedures; Review analytical and manufacturing recordsdocumentation in support of quality oversight for the clinical products; review root cause analysis and approve product quality investigations, out of specification results, and product complaints; verify compliance for development activities with applicable regulations. Up to 20 travel required. Up to 40 telecommuting allowed; must live within normal commuting distance of Cambridge, MA.
Categories: eb3
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