Job Description
Job Title
Documentation Control Specialist (GMP Environment)
Sector
Pharmaceutical / Life Sciences / Manufacturing
Role
Supports the execution and management of company documentation, including collecting, verifying, and processing documents in line with internal procedures. Ensures documents are properly approved, signed, and stored within the document management system. Handles administrative tasks such as scanning, indexing, and archiving. Contributes to compliance with GMP standards, particularly in raw material release processes.
Non‑Negotiable Skills, Qualifications, and Experience
- 1–3 years of professional experience in a relevant role
- Experience with GMP (Good Manufacturing Practice) documentation processes
- Experience releasing raw materials based on Certificates of Analysis (CoA)
- Experience handling TSE/BSE documentation updates
- Proficiency in English (written an...