Global QP: Pharma Quality & Batch Release (France)

Air Products Inc.; Lille; Hybrid; EUR 70,000 - 95,000; Full time

Job summary

Air Products is seeking a Qualified Person (QP) for the Templemars site in Lille, France. You will ensure GMP-compliant operations and certify batches of medicinal gases for distribution, reporting to Pharmacien Responsable as required.

This role offers an international environment and a strong emphasis on patient safety and regulatory compliance. The successful candidate will hold a Master's in Pharmacy, have at least 2 years in pharma quality/manufacturing, and be proficient in English, with a

Qualifications

• Masters degree in Pharmacy and eligibility to act as a QP in France.
• Minimum 2 years of pharmaceutical industry experience in Quality, Manufacturing, QC, or Compliance.
• Strong knowledge of EU GMP and pharmaceutical quality systems.
• Experience with batch certification and release activities.
• Familiarity with regulatory inspections and health authority interactions.
• Excellent communication and stakeholder management skills.

Responsibilities

• Act as site Qualified Person and certify/release batches of medicinal gases.
• Ensure operations meet GMP, regulatory, and approved specifications.
• Maintain and improve the Pharmaceutical Quality Management System.
• Lead and support internal and external audits and regulatory inspections.
• Collaborate with cross-functional teams to drive quality and compliance.
• Escalate significant quality or regulatory issues as needed.
• Support CE marking compliance for applicable medical devices.

Skills

Quality management

Audits & compliance

GMP knowledge

Regulatory inspections

English proficiency

Education

Masters Degree in Pharmacy

Job description

Air Products is seeking a Qualified Person (QP) for the Templemars site in Lille, France. You will ensure GMP-compliant operations and certify batches of medicinal gases for distribution, reporting to Pharmacien Responsable as required.

This role offers an international environment and a strong emphasis on patient safety and regulatory compliance. The successful candidate will hold a Master's in Pharmacy, have at least 2 years in pharma quality/manufacturing, and be proficient in English, with a