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
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