Global QP - GMP Compliance & Batch Release Leader

Air Products S.A.S (FR); Lille; On-site; EUR 90,000 - 120,000; Full time

Job summary

Air Products S.A.S (FR) seeks an experienced Qualified Person (QP) to certify and release medicinal gas batches at the Templemars site in France. You will ensure GMP compliance, maintain the Pharmaceutical Quality Management System, and support regulatory inspections in a highly collaborative, international environment.

The ideal candidate holds a Masters in Pharmacy, at least 2 years in quality/ manufacturing, and strong EU GMP knowledge, with fluent English and a valid driving license.

Qualifications

• Masters Degree in Pharmacy with eligibility to act as QP in France.
• Minimum 2 years in Quality, Manufacturing, Quality Control, or Compliance.
• Strong knowledge of EU GMP requirements and pharmaceutical quality systems.
• Experience with batch certification and release activities.

Responsibilities

• Act as the site's Qualified Person (QP) ensuring GMP compliance.
• Certify and release batches of medicinal gases for distribution.
• Ensure manufacturing, testing and QC meet specifications and regs.
• Maintain and improve the Pharmaceutical Quality Management System.
• Lead audits and support regulatory inspections and health authority interactions.
• Collaborate with cross-functional teams to drive quality and compliance.
• Escalate significant quality/regulatory issues to the Pharmacien Responsable.
• Support quality requirements related to CE-marked medical devices when applicable.

Skills

Quality management

Regulatory compliance

Auditing

Stakeholder management

English proficiency

Driver's license

Education

Masters Degree in Pharmacy

Job description

Air Products S.A.S (FR) seeks an experienced Qualified Person (QP) to certify and release medicinal gas batches at the Templemars site in France. You will ensure GMP compliance, maintain the Pharmaceutical Quality Management System, and support regulatory inspections in a highly collaborative, international environment.

The ideal candidate holds a Masters in Pharmacy, at least 2 years in quality/ manufacturing, and strong EU GMP knowledge, with fluent English and a valid driving license.