QA

The role supports quality oversight of external manufacturers (CMOs) producing clinical trial products, within a highly matrixed, global environment. The position is non‑signature and does not include decision‑making authority.

• Job Title: QA / Clinical Quality Support Contractor
• Contract: 1.5 years | Full‑time (40 hours/week) | Immediate start

Key Responsibilities

• Review and check controlled quality documentation (no approval/signature)
• Ensure correct use of templates, formats, and documentation standards
• Support QMS activities including deviations, CAPAs, and change controls
• Support audit and inspection readiness activities
• Maintain quality metrics, trackers, and reporting outputs
• Support risk management and training documentation
• Provide general QA and process optimisation support across the network

Requirements

• 1-3 years' experience in QA, Clinical Quality, or GMP environments
• Exposure to QMS documentation (deviations, CAPAs, change control)
• Pharmaceutical or biotech background
• Strong written and verbal English
• Comfortable working in a global, stakeholder‑heavy environment
• Based in, or able to work in, a Central European time zone