Description
Amgen is hiring a GMP Manufacturing Documentation Specialist to support the manufacturing team by developing, reviewing, and maintaining SOPs, work instructions, protocols, technical reports, training materials, and quality records. The role also supports deviations, CAPAs, change controls, quality risk management, troubleshooting, continuous improvement, and GMP compliance. Candidates need a doctorate or an equivalent combination of degree and experience in engineering, manufacturing, packaging, or quality within pharmaceutical, medical device, or biotechnology companies, with GMP and technical-writing experience preferred.
