GCP Quality Manager (12 Contract)
| Company: | Hays Specialist Recruitment |
|---|---|
| Salary: | Not specified |
| Hours: | Full-time |
| Location: | OX1 3PA |
| Working pattern: | Hybrid - 3 days remote |
| Job type: | Contract |
| Posting date: | 23 Sept 2026 |
| Closing date: | 30 Sept 2026 |
Summary
Your new company
A research-driven life sciences organisation focused on advancing innovative therapies through clinical development and commercial growth. The business operates within a highly regulated global environment and combines scientific expertise with a patient-focused approach to bring new treatment options to market. With a growing pipeline and continued investment in its operations, this is an opportunity to join a company at an exciting stage of its development journey.
Your new role
- As a Quality Manager, you will provide quality oversight across clinical activities and the Quality Management System (QMS). You will lead and support internal, external and vendor audits, manage quality events, CAPAs and root cause investigations, and contribute to regulatory inspection readiness activities. Working cross-functionally with Clinical Operations, Pharmacovigilance, Regulatory Affairs and Quality teams, you will help drive compliance across GCP, GCLP and GVP activities while supporting continuous improvement initiatives.
What you'll need to succeed
- Significant experience within Quality Assurance in the pharmaceutical, biotechnology or clinical research sectors.
- Strong knowledge of GCP, GCLP and GPvP requirements.
- Experience conducting internal, external and supplier audits.
- Working knowledge of Quality Management Systems, CAPAs, deviation management, RCA and risk management tools.
- Experience supporting regulatory inspections and inspection readiness activities.
- Strong stakeholder management, communication and influencing skills.
- Experience working within a fast-paced clinical development, pharmaceutical or biotech environment.
- Familiarity with eQMS platforms such as VeevaVault, TrackWise or MasterControl would be advantageous
- Hybrid working is possible, with a regular on-site presence. Applicants within reasonable commuting distance of the site are strongly encouraged to apply.
What you'll get in return
- Competitive day rate contract opportunity inside IR35.
- The opportunity to work within a cutting-edge life sciences organisation delivering innovative therapies.
- Exposure to a broad range of clinical quality activities covering GCP, GCLP and GPvP.
- A collaborative environment with significant stakeholder interaction across multiple business functions.
- Flexible hybrid working arrangements with some on-site presence required.
- The chance to make a meaningful impact on quality and compliance across global clinical development programmes
What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career.
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