GMP & FDA Technical Writer: Validation & Docs; On-Site
Listed on 2026-09-30
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Quality Assurance - QA/QC
Regulatory Compliance Specialist
Alcami Corporation is seeking a Technical Writer to develop FDA- and GMP-compliant documentation supporting pharmaceutical packaging operations, including Master Batch Records (MBRs), validation tests, and qualification activities. The role requires clear communication to diverse stakeholders and collaboration across teams to ensure compliant, traceable documentation in a regulated environment.
The position is on-site with standard daytime hours, focused on on-site execution and continuous
This posting is for the GMP & FDA Technical Writer:
Validation & Docs (On-Site) role at Alcami Corporation, based in MI, United States.
Join Alcami Corporation and contribute to our ongoing work.
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We are looking to fill the GMP & FDA Technical Writer:
Validation & Docs (On-Site) position at Alcami Corporation in MI, United States.
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