Sr Manager GXP Technical Investigations/Writing (JMR)
Job Location: Parsippany, NJ
Date Posted: 2020-01-15
Growing Biotech Company needs someone to lead a team of technical investigators to support clinical documentation. Will work with QA teams to determine appropriate CAPA, create
evise SOP’s, qualification/validation protocols, and risk assessments. Will review, author, and manage investigations, write GXP reports, utilize root cause analysis during deviation investigations, and assist in BLA submission writing. Will need 6+ years experience in investigations, root cause analysis, and GXP regulations.
Please contact Joe Raia at email@example.com
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