Internship - MSAT Validation & Control (m/fd)

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.

Start date: Sept / Oct 2026

Duration: 6 months

Localisation: Corsier-sur-Vevey

Role level: Internship

Your role:

During this internship, you will:

• Review and assess historical WCB validation activities performed at the Vevey manufacturing site.
• Analyze current practices and identify opportunities for harmonization and standardization.
• Develop a scientifically sound and regulatory-compliant validation strategy applicable to all WCBs.
• Evaluate the potential benefits of the proposed approach, including efficiency gains and reduction of validation workload.
• Collaborate with MSAT and cross-functional stakeholders to support the implementation of the strategy.
• Present findings, recommendations, and project outcomes to the team.

Your profile:

• Currently enrolled in a Master's degree or Engineering program in Biotechnology, Life Sciences, Bioprocess Engineering, Chemical Engineering, or a related field.
• Strong interest in biopharmaceutical manufacturing and validation activities within a GMP-regulated environment.
• Curious, proactive, analytical, and eager to learn.
• Able to work independently while collaborating effectively within a multidisciplinary team.
• Strong communication and presentation skills.
• Fluent in English; French is an asset.

What we offer: 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!