C&Q Document Preparation Support (Drug Substance)
Amgen · Hyderabad, India
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Role summary
Amgen seeks a Senior Associate to develop commissioning and qualification documentation for engineering projects and GMP manufacturing systems, primarily supporting drug substance operations. The role involves authoring protocols, reports, and related lifecycle documents while coordinating with cross-functional teams to ensure compliance and regulatory readiness. Candidates should have GMP documentation experience, preferably in biotechnology manufacturing systems and capital projects.
Privacy & handoff
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