Senior Qualified Person (QP) – GMP Compliance & Release Leader

Air Products; Lille; On-site; EUR 70,000 - 110,000; Full time

Job summary

Air Products seeks a qualified person (QP) to oversee GMP-compliant pharmaceutical operations at the Templemars site in France. You will certify batches, ensure QC and manufacturing meet regulatory standards, and maintain the Pharmaceutical Quality Management System while leading audits and coordinating inspections.

With a focus on strong English communication and cross-functional teamwork across Europe, this role supports ongoing compliance and quality improvements within a global industrial

Qualifications

• Masters Degree in Pharmacy and eligibility to act as a Qualified Person (QP) in France.
• Minimum 2 years of pharmaceutical industry experience within Quality, Manufacturing, Quality Control, or Compliance.
• Strong knowledge of EU GMP requirements and pharmaceutical quality systems.

Responsibilities

• Act as the site's Qualified Person (QP) and ensure continued compliance with pharmaceutical regulations and GMP requirements.
• Certifying and releasing batches of medicinal gases for commercial distribution.
• Ensuring manufacturing, testing, and quality control activities meet approved specifications and regulatory requirements.
• Maintaining and continuously improving the Pharmaceutical Quality Management System.
• Leading and supporting internal and external audits to ensure ongoing compliance.
• Preparing for, coordinating, and supporting regulatory inspections.
• Working closely with cross-functional teams to drive quality and compliance across the site.
• Escalating significant quality or regulatory issues to the Pharmacien Responsable when required.
• Supporting compliance with quality requirements related to CE-marked medical devices when applicable.

Skills

Strong communication

Stakeholder management

English proficiency

Education

Master's Degree in Pharmacy

Job description

Air Products seeks a qualified person (QP) to oversee GMP-compliant pharmaceutical operations at the Templemars site in France. You will certify batches, ensure QC and manufacturing meet regulatory standards, and maintain the Pharmaceutical Quality Management System while leading audits and coordinating inspections.

With a focus on strong English communication and cross-functional teamwork across Europe, this role supports ongoing compliance and quality improvements within a global industrial