Pharma Packaging Technical Writer — Validation & GMP Docs
Listed on 2026-09-30
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Pharmaceutical
Pharmaceutical Manufacturing, Validation Engineer, Pharma Engineer, Pharmaceutical Science/ Research
Alcami is seeking a Technical Writer to join our Technical Services team on a 100% on-site, first-shift basis. You will author FDA- and GMP-compliant documentation, including Master Batch Records (MBRs), validation tests for equipment and components, and support qualification activities for new products and validated packaging operations.
The ideal candidate has at least two years of pharma cGMP writing experience, strong communication skills, and proficiency with Office 365 tools.
We have an opening for a Pharma Packaging Technical Writer — Validation & GMP Docs in MI, United States within Bio & Pharmacology & Health, Engineering.
This role, Pharma Packaging Technical Writer — Validation & GMP Docs at Alcami-5, could be your next career step.
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