Qualified Person (QP)

Qualified Person (QP) - IMPs

Connected MedTech is partnering exclusively with a specialist pharmaceutical organisation to appoint a Qualified Person (QP) into a key role within its Quality function.

Operating within a GMP-regulated manufacturing environment, the position will support the certification and release of pharmaceutical products manufactured for clinical trial supply.

This opportunity offers the chance to join a respected pharmaceutical manufacturer specialising in the development and production of investigational medicinal products. The role offers significant involvement across Quality, Manufacturing and Technical Operations, making it an attractive opportunity for a QP seeking both variety and the opportunity to influence the wider business.

The Role

The successful candidate will work closely with Quality, Manufacturing and Technical Operations teams, providing GMP expertise and supporting the ongoing development of quality and operational systems within a fast-paced manufacturing setting.

Key responsibilities:

• QP certification and release activities for products manufactured for clinical trial supply
• Supporting GMP compliance across manufacturing operations
• Participation in audits, inspections, investigations and CAPA activities
• Providing QA and regulatory guidance across technical teams
• Supporting quality system and operational improvement initiatives

About You

The ideal person will demonstrate:

• Eligibility to act as a UK Qualified Person
• Significant experience working within UK GMP-licensed pharmaceutical manufacturing environments, particularly supporting IMPs and sterile products
• Strong stakeholder engagement and decision-making capability
• Ability to operate effectively within a collaborative technical environment

For further information or a confidential discussion, please get in touch.