Qualified Person (QP) - Sterile Manufacturing
Are you a Qualified Person with experience in sterile pharmaceutical manufacturing? Looking to make an impact in a forward-thinking company where quality and patient safety come first?
Smart4 Sciences are working with a pharmaceutical manufacturer in Essex specialising in the production of sterile and non-sterile products. As part of their continued expansion, they're seeking an experienced and proactive Qualified Person to join their quality team.
**The Role:
As a QP, you'll be responsible for ensuring that products released to market meet the highest standards of GMP compliance and patient safety. Working in a modern GMP facility, you will:
- Act as a QP for the certification and release of sterile pharmaceutical products
- Ensure full compliance with MHRA and EU GMP guidelines
- Liaise closely with QA, Production, and Regulatory Affairs teams
- Contribute to audits, inspections, and continuous improvement projects
- Support the development of junior QA staff and provide QP oversight where needed
**About You:
- Eligible to act as a Qualified Person under Directive 2001/83/EC
- Prior experience working with sterile manufacturing (aseptic/terminally sterilised products) is desirable
- Strong working knowledge of EU GMP and UK pharmaceutical regulations
If you're a QP ready for your next challenge in a state-of-the-art sterile manufacturing environment, we'd love to hear from you!
Apply today or contact Gareth Gooley on for a confidential discussion.