Onsite GMP Technical Writer - SOPs & Control Expert
Listed on 2026-10-07
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Pharmaceutical
Pharmaceutical Manufacturing -
Quality Assurance - QA/QC
Planet Pharma onsite in Clayton, NC seeks a pharmaceutical technical writer to create, revise, and manage GMP documentation supporting manufacturing operations, process engineering, facilities, training, and quality systems.
This role goes beyond editing; you will translate complex production activities into clear written instructions, author SOPs, work instructions, and controlled documents, and work with SMEs to ensure accuracy and compliance.
The Onsite GMP Technical Writer - SOPs & Change Control Expert position in the Bio & Pharmacology & Health, Engineering field is open for applications.
We have an opening for a Onsite GMP Technical Writer - SOPs & Change Control Expert in Clayton, NC, United States within Bio & Pharmacology & Health, Engineering.
This role, Onsite GMP Technical Writer - SOPs & Change Control Expert at Planet Pharma, could be your next career step.
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