GMP Technical Writer: Deviation & Compliance Lead
Randstad USA
Randstad USA is seeking a candidate in Norwood, Massachusetts, to support GMP manufacturing operations by managing technical documentation and deviation investigations. You will partner with various teams to ensure compliance with cGMP regulations and contribute to manufacturing readiness. The ideal candidate should possess a technical degree along with extensive experience in the pharmaceutical or biotechnology sectors, particularly in deviation investigations and technical writing. This role is site-based with no remote work allowed. #J-18808-Ljbffr Randstad USA
Vacancy posted 2 days ago
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