We are looking for an experienced Qualified Person (QP) to join a Nottingham-based team on a permanent basis. This is an exciting opportunity to work with a global pharmaceutical company that offers a strong benefits package and a collaborative environment focused on quality and innovation.
Key Responsibilities
- Act as a Qualified Person in accordance with EU and UK regulations, ensuring compliance with GMP standards.
- Certify batches for release to market, maintaining the highest standards of product quality and patient safety.
- Provide expert guidance on quality systems, regulatory compliance, and continuous improvement initiatives.
- Collaborate with cross-functional teams to support manufacturing and supply chain operations.
- Contribute to audits and inspections, ensuring readiness and compliance at all times.
Requirements
- Current eligibility and registration as a Qualified Person under UK/EU law.
- Strong knowledge of GMP and pharmaceutical quality systems.
- Experience within sterile pharmaceutical manufacturing is highly desirable.
- Excellent communication and problem-solving skills.
- Ability to work effectively in a global, fast-paced environment.
What’s on Offer
- Competitive salary and comprehensive benefits package.
- Permanent position within a global organization committed to quality and innovation.
- Opportunities for professional development and career progression.
Ready to take the next step?
Apply today and become part of a global team dedicated to improving patient outcomes worldwide!