Qualified Person (QP) - Pharmaceutical Manufacturing

AirProducts; Lille; Hybrid; EUR 90,000 - 130,000; Full time

Job summary

Air Products is seeking a Qualified Person (QP) for our Templemars manufacturing facility in France. You will certify and release batches of medicinal gases, ensure GMP compliance, and maintain the Pharmaceutical Quality Management System.

You will work with cross-functional teams to uphold regulatory standards and support audits and inspections in an international environment. The role requires a Master’s in Pharmacy, at least 2 years in pharma quality/compliance, EU GMP knowledge, and English

Qualifications

• Masters Degree in Pharmacy and eligibility to act as a Qualified Person (QP) in France.
• Minimum 2 years of pharmaceutical industry experience in 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.

Responsibilities

• Act as the site's Qualified Person (QP) and ensure GMP compliance.
• Certify and release batches of medicinal gases for commercial distribution.
• Ensure manufacturing, testing, and quality control meet specs and regulatory requirements.
• 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.

Skills

GMP knowledge

Quality management

Regulatory compliance

Auditing experience

Stakeholder management

English proficiency

Education

Masters Degree in Pharmacy

Job description

## Qualified Person (QP) - Pharmaceutical ManufacturingSolicitar: Lille, France: Jornada completa: Publicado ayer: JR-2026-22751En Air Products, reimaginamos lo que es posible. Aprovechando la motivación de nuestra gente y nuestra experiencia colectiva, creamos las ideas y las innovaciones que nos impulsan hacia adelante. Cuando nos unimos —en un entorno donde se escucha cada voz y todos saben que forman parte del equipo y que son importantes— creamos soluciones que lanzan a las personas al espacio, respaldan la atención médica vital en los hospitales y permiten la construcción de instalaciones de producción pioneras a escala mundial. Reimaginemos lo que es posibleAs 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.This is an excellent opportunity for an experienced pharmaceutical professional **who is passionate about GMP compliance, quality excellence, and patient safety, and who enjoys working in an international environment**. **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.**Your key responsibilities will include:*** **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.**Interested? We'd love to hear from you. Apply today and become part of a team where quality, compliance, and patient safety are at the heart of everything we do.**#LI-MJ1Fundada en 1940, Air Products es una empresa líder mundial en gases industriales y cuenta con una orgullosa trayectoria de innovación y excelencia operativa, con un compromiso inquebrantable con la seguridad y la gestión medioambiental. Trabajando juntos, aprovechamos nuestra pasión y nuestros diversos orígenes para reimaginar lo que es posible y generar un futuro más limpio para nuestros clientes, nuestras comunidades y el mundo.