Qualified Person (QP) - Pharmaceutical Manufacturing

Air Products; Lille; Presencial; EUR 70.000 - 110.000; Jornada completa

Descripción de la vacante

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

Formación

• 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.

Responsabilidades

• 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.

Conocimientos

Strong communication

Stakeholder management

English proficiency

Educación

Master's Degree in Pharmacy

Descripción del empleo

At Air Products, we reimagine what's possible. By tapping into the motivation of our people and our collective experience, we create the ideas and innovations that drive us forward. When we come together - where every voice is heard and everyone knows they belong and matter - we create solutions that launch people into space, support lifesaving care in hospitals, and enable the construction of groundbreaking, world scale production facilities.

Reimagine What's Possible

As a Qualified Person (QP ), you will play a critical role in ensuring the quality, safety, and compliance of medicinal gases manufactured at our Templemars site in France.

What you will be doing

As the Qualified Person for our Templemars manufacturing facility, you will be responsible for ensuring that pharmaceutical operations are performed in compliance with GMP requirements , Marketing Authorisations, Manufacturing Authorisations, and applicable French and EU pharmaceutical regulations.

• Acting as the site's Qualified Person (QP) and ensuring 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.

What you will Bring

• 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.
• Experience with batch certification and release activities.
• Familiarity with regulatory inspections and health authority interactions.
• Excellent communication and stakeholder management skills.
• Professional proficiency in English .
• Valid driver's license.

Why join Air Products?

• Take ownership of a highly impactful and visible QP role.
• Be part of international environment with opportunities to collaborate across Europe.
• Contribute to products that support healthcare and improve patient lives every day.

Founded in 1940, Air Products is a world-leading industrial gases company and has a proud history of innovation, operational excellence, with an unwavering commitment to safety and environmental stewardship. Working together, we are taking our passion and diverse backgrounds forward to reimagine what's possible and generate a cleaner future for our customers, our communities, and the world.