QA Operations Associate Manager

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.

Ensure GMP compliance across all operational activities at the Vevey site—Buffers & Media Production, Engineering & Maintenance, Warehouse, and Data & Digital—so that products manufactured, tested, and stored meet Quality Standards and cGMP. Contribute to continuous improvement and provide QA services aligned with market needs and the site’s strategy.

• Manage and organize the QA OPS support within the assigned scope; lead meetings, track actions, and coach team members.
• Ensure compliance of areas and activities (GMP/cGMP, quality procedures) and alignment with other sites.
• Lead deviation management (T&T/minor/major); escalate major cases, identify recurrence, and define/follow CAPAs.
• Contribute to change control, risk management (drafting, review, approval), and GMP document updates.
• Coordinate investigations with involved departments; ensure a pragmatic, results‑oriented approach.
• Participate in internal/external audits and inspections; present quality topics to partners and authorities.
• Strengthen cross‑department collaboration and develop the team’s quality expertise (training, coaching).
• Deliver projects with high impact on quality/GMP on time and to the expected standard.

• Advanced technical/science/engineering degree (e.g., Pharm
  
  D, Engineer) or equivalent experience.
• Significant Quality Assurance experience in a GMP environment.
• Strong command of GMP rules, quality systems, and production IT/systems.

• Leadership, teamwork, impactful communication, results orientation, customer focus.
• Ability to adapt to change, coordinate cross-functionally, resolve conflicts, and identify risks.

• French: fluent
• English: fluent (multi‑site interactions, clients/partners, auditors/authorities)

We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety 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 a team that is dedicated to Sparking Discovery and Elevating Humanity!