Qualified Person (QP) - Pharmaceutical Manufacturing

Air Products Inc.; Lille; Hybrid; EUR 70.000 - 95.000; Vollzeit

Zusammenfassung

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

Qualifikationen

• 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.

Aufgaben

• 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.

Kenntnisse

Quality management

Audits & compliance

GMP knowledge

Regulatory inspections

English proficiency

Ausbildung

Masters Degree in Pharmacy

Jobbeschreibung

## Qualified Person (QP) - Pharmaceutical Manufacturing應徵: Lille, France: Full time: 昨天刊登: JR-2026-22751在安瑞普特,我們重新定義可能性。透過激發員工的熱情並匯聚集體經驗,我們孕育出推動公司前進的創意與創新。當我們齊心協力——在每個人的聲音都能被傾聽、每個人都深知自己歸屬且重要的環境中——我們所創造的解決方案,不僅能將人類送入太空、支援醫院的救命照護,更能推動開創性的全球級生產設施建設。 重新定義可能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.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-MJ1