Pharma Packaging Technical Writer — Validation & GMP Docs
Listed on 2026-11-01
-
Pharmaceutical
Regulatory Compliance Specialist, Pharmaceutical Manufacturing -
Quality Assurance - QA/QC
Regulatory Compliance Specialist
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.
Our organisation is growing, and we are hiring a Pharma Packaging Technical Writer — Validation & GMP Docs in MI, United States.
All applications are reviewed carefully by our team.
The position is based in MI, United States.
This opportunity is part of our work in Bio & Pharmacology & Health, Engineering.
The advertised compensation is 65.000 - 85.000.
We aim to respond to suitable candidates as soon as possible.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).