Qualified Person
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- 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 doingAs 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
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