Job Description
Location: London area (3-4 days on site)
Salary: £60,000–£90,000
ReeVR Talent are partnering with an innovative, highly regulated sterile manufacturing business looking to appoint an experienced Quality Manager.
This is a fantastic opportunity for a strong Quality leader to take ownership of a multi-faceted Quality function, leading teams across QA, Auditing and Validation.
You will play a key role in driving GMP compliance, strengthening quality systems and embedding a proactive quality culture across the wider manufacturing operation.
Key responsibilities- Lead and develop multi-disciplinary Quality teams across QA, Auditing and Validation.
- Drive and continuously improve the site''s Quality Management System.
- Ensure GMP compliance and maintain inspection readiness.
- Lead regulatory inspections, customer audits and internal audit programmes.
- Oversee deviations, CAPAs, change controls and investigations.
- Provide quality oversight across sterile manufacturing and aseptic operations.
- Monitor quality KPIs and drive continuous improvement.
- Partner with Manufacturing, Engineering and Technical Operations to embed quality across the site.
- Develop people, strengthen accountability and build a high-performing Quality function.
- Proven Quality leadership experience within pharmaceutical, sterile or highly regulated manufacturing.
- Strong knowledge of GMP, QMS and regulatory requirements, ideally including EU GMP Annex 1.
- Experience managing and developing multi-disciplinary teams.
- Strong background in audits, inspections, CAPAs and quality systems.
- A track record of driving quality culture and continuous improvement.
- Confident stakeholder management and the ability to influence across all levels.
If you''re a hands-on Quality leader who can bring teams together, drive standards and champion quality across a sterile manufacturing environment, we''d love to hear from you!
Due to a high level of applications, if you do not hear from us within 5 working days, please assume your application has been unsuccessful.