QA Engineering & R&D Projects Manager (m/f/d)

Posted 31 Jan 2023

Aubonne, Vaud - Switzerland

Req Id 259468


Work Your Magic with us!

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.


In this role, you will manage a team of professional which purpose is to ensure compliance with cGMP and our company standards for all engineering projects of the sites (facilities, utilities, equipments, CSV). You will drive compliance with cGMP and our standards for all qualification, validation and maintenance activities. You will also work towards the release of clean utilities (gaz and water).


Your Role

You manage the QA engineering and the QA SKY team (a new building).

You ensure adequate recruitment and training of all team members.

You ensure inspection readiness of areas in scope of activities, supporting teams during the inspections

You manage employee development and performance management process.

You ensure compliance with internal and external regulations

You ensure QA supervision and support of engineering projects

You support the Site Management to achieve our site objectives.

You continuously improve organization and processes to reach high level of performance in all areas.


Who you are

  • You bring 10-15 years of experience of sterile products manufacturing in the pharmaceutical industry, in QA or in production
  • You bring expertise in cGMP in the areas of pharmaceutical technology, engineering, aseptic filling, qualification, calibration and sterilization
  • You are well-versed in the implementation of a lean quality management system within the pharmaceutical sector
  • You hold an Engineer degree or equivalent
  • You are fluent in French and English

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
Apply now and become a part of our diverse team!

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