AssureBio is working with an established manufacturer in the radiopharmaceutical space to find an experienced Qualified Person (QP) to join their Quality function.
This role combines hands-on batch release with a leadership stake in the site's Quality Management System, ideal for a QP ready to broaden their scope beyond pure release.
What's involved:
- Batch release of medicinal products, ensuring full regulatory compliance
- Review and sign-off of batch records, analytical data and supporting documentation
- Leading investigations into deviations and quality issues
- Representing Quality at internal and regulatory audits
- Advising internal teams on regulatory and quality standards
- Contributing to ongoing QMS development and management
What you'll bring:
- A science degree (chemistry, pharmacy, biology or related)
- Eligible QP (UK)
- Minimum 3 years' hands-on experience in the quantitative/qualitative testing of active substances and medicinal products
- QP release experience within sterile manufacturing, radiopharmaceutical or nuclear medicine background strongly advantageous
- Some experience managing a QMS or a Quality team
Locations
Qualified Person in Cheshire, Warrington employer: AssureBio
AssureBio is an exceptional employer, offering a dynamic work environment where innovation meets compliance in the pharmaceutical sector. With a strong focus on employee growth and development, we provide comprehensive training and support for our team members, ensuring they thrive in their roles while contributing to meaningful projects that impact global health. Our collaborative culture, combined with the opportunity to lead significant operational transformations, makes this an ideal workplace for those seeking a rewarding career in a regulated industry.
