Qualified Person (QP)
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 growing pharmaceutical organisation with a strong technical focus, modern manufacturing capabilities and a collaborative approach across Quality, Manufacturing and Technical Operations.
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 profile will include:
* 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.