Quality Manager / Deputy Responsible Person - all genders -
Rotkreuz, 瑞士 Regular 发布于 Jun. 17, 2026 申请截止于 Jul. 02, 2026To ensure a rapid processing of your application, please apply only via the “Apply” button. Please include a letter of motivation and a current resume with your application.
About the job
As Quality Manager and Deputy Responsible Person within our Swiss Quality Team, you are a key guardian of patient safety — driving quality excellence, ensuring regulatory compliance, and shaping the quality culture across our Swiss operations. Ready to get started?
At Sanofi Switzerland, our Quality Team exists for one reason: to ensure that every patient receives a safe, effective, and high-quality medicine. We are a passionate, collaborative team of quality professionals responsible for GMP/GDP compliance, the maintenance of a robust Quality Management System (QMS), and the release and distribution of medicinal products to the Swiss market. As the primary interface with Swissmedic for all quality-related matters, we play a critical role in upholding Swiss regulatory standards while supporting Sanofi's global launch platform.
About Sanofi:
We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.
Main responsibilities:
- Act as Deputy Responsible Person for wholesale, import/export, and trading abroad activities in accordance with Swiss MPLO regulations (812.212.1), in the absence of or as delegated by the Responsible Person
- Partner with the RP to establish and continuously improve a robust, compliant Quality Management System aligned with Sanofi Global and Swiss regulatory requirements
- Independently manage market batch releases, deviations, returns, and destructions with a high degree of accountability and precision
- Support the Responsible Person in communications with Swissmedic and other health authorities, and actively prepare for and manage health authority inspections and internal quality audits
- Lead CAPA responses to inspection and audit findings, ensuring timely and effective resolution with thorough documentation
- Ensure quality oversight of third-party partners involved in GDP/GMP activities, including quality agreements and risk-based audits
- Review and approve documents within the RP's area of responsibility, ensuring full compliance with Swiss regulations and driving proactive Quality Risk Management initiatives
- Drive a strong quality culture across all functions, providing leadership and guidance on quality standards, processes, and GDP requirements while representing quality in cross-functional projects
About you
Experience:
- Several years of progressive, hands-on experience in a pharmaceutical quality environment (GMP/GDP)
- Solid, demonstrable knowledge of Swissmedic requirements, EU GMP, and EU GDP regulations
- Proven experience with batch release, deviation management, and CAPA processes
Soft and technical skills:
- Strong decision-making capabilities in fast-paced, innovative environments
- Demonstrated leadership skills with the ability to drive quality mindset and organizational change
- Excellent interpersonal and communication skills, with experience working across diverse cultures and functions
- Open-minded, continuous improvement orientation with a proactive approach to problem-solving
Education:
- University degree in Life Sciences or Pharmacy
Languages:
- Excellent command of German and English, both written and spoken
Why choose us?
- Find diverse opportunities in an international work environment to develop your talent professionally and personally, and to continuously advance your career through internal changes and role expansions. A personalized and structured onboarding is a given and begins even before your first day.
- Our employees are our top priority, especially when it comes to work-life balance and an inclusive work environment. In addition to flexible working, we offer our employees flexible working hours and a hybrid work model (3 days in the office/2 days remote).
- Outstanding is our 14-week paid family time after the birth of a child for both parents, as well as additional benefits such as health insurance, mental and physical health offerings, and leave for caregiving relatives.
- Training opportunities and international career possibilities round out our offerings.
#LI-Hybrid
#LI-GSA
null追寻 发展。探索 菲凡。
进步需要我们每个人的参与——不论其背景、地域、或职业,我们都有一个共同的愿望:创造奇迹。你也可以成为其中的一员。我们不断追求变革,拥抱新思想,探索我们所能提供的一切机会。让我们一起追求进步。共同发现非凡。
在赛诺菲,不分种族、肤色、血统、宗教、性别、国籍、性取向、年龄、公民身份、婚姻状况、残疾或性别认同,我们为所有人提供平等的机会。
观看 “在赛诺菲的一天” ,并在官网 (sanofi.com) 上查看赛诺菲的多元化、公平与包容倡议!
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