About this opportunity
Alcami Corporation lists this GMP & FDA Technical Writer: Validation & Docs (On-Site) opportunity in northern, Kentucky. Review the employer’s description below for duties, qualifications and application requirements.
Job description
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
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Who can apply
Review the original listing for work authorization, qualifications and employer requirements.