Qualified Person

I am currently supporting a leading CDMO who are looking to appoint an experienced Qualified Person (QP) to join their Quality team in France.

This is a key position within the organisation, with responsibility for ensuring the safe and compliant release of medicinal products in line with EU GMP requirements .

Key responsibilities

• Certification and release of batches in accordance with EU GMP
• Ensuring ongoing compliance with regulatory requirements and quality standards
• Supporting regulatory inspections and quality initiatives
• Reviewing deviations, investigations, CAPAs and change controls
• Working closely with Manufacturing, Quality, Regulatory and Supply Chain teams

Ideal experience

• Qualified Person status (EU) with experience operating within a GMP environment
• Strong pharmaceutical manufacturing background
• Experience with batch release and quality decision-making
• Good understanding of EU GMP regulations and regulatory expectations
• Ability to collaborate effectively across cross-functional teams

This is an excellent opportunity for a QP looking to join a respected pharmaceutical organisation and play a key role in ensuring product quality and patient safety.