An international life sciences organisation is seeking a Document Control Specialist to support Quality and Raw Materials activities within a GMP‑regulated environment. The role focuses on documentation review, compliance checks, and data management to support timely material release.

Key Responsibilities:

• Review and control raw materials documentation (CoA, TSE/BSE)
• Verify approvals and authorised signatures
• Update, archive, and maintain documents in electronic document management systems
• Scan, index, upload, and ensure traceability of controlled records

Requirements:

• 1–3 years’ experience in document control, quality operations, or GMP environments
• Exposure to raw materials documentation (CoA, TSE/BSE) preferred
• Working knowledge of GMP
• Business‑fluent English required; German is an advantage