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Senior Digital Compliance Expert (m/f/d)

 

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.

 

Your role :

We are looking for a Senior Digital Compliance Expert who wants real ownership, visible impact, and the autonomy to drive critical compliance topics in a GMP-regulated environment.

Digital is one of the most dynamic and fast-growing areas in our environment, and the compliance framework around it is still being shaped. This role offers the opportunity to take real ownership in that space — building, strengthening, and raising the standard of digital compliance where it matters most.

This role is for someone who combines strong compliance & CSV expertise, especially in investigations, with leadership, sound judgment, and the resilience to perform in high-stakes situations.

  • Lead and strengthen deviation investigations, including impact assessment, root cause analysis, documentation quality, and robust CAPA definition

  • Maintain the validated status of computerized and automated systems, including periodic reviews and qualification activities

  • Initiate and coordinate Change Control Processes and associated risk assessments

  • Support audit and inspection readiness and act as SME when required

  • Raise the standard of compliance deliverables, ensuring they are clear, focused, and inspection-ready

  • Drive continuous improvement in compliance processes, data integrity, and operational quality practices

  • Influence cross-functional stakeholders and help shape the right quality decisions

Who you are:

  • Proven compliance experience in a biopharma or similarly regulated environment, with strong hands-on expertise in investigations

  • Solid knowledge of GMP / CSV requirements, with strong practical knowledge of computerized system lifecycle management and risk-based validation approaches (e.g. GAMP 5), including validation of complex automated and manufacturing systems.

  • Good practical understanding of GMP computerized or automated systems (such as DCS/SCADA, MES, ERP/SAP, historians or laboratory systems) and biopharma manufacturing processes

  • Strong leadership presence and the ability to influence credibly in a matrix environment

  • An excellent mindset: resilient, collaborative, accountable, and solution-oriented

  • Clear, concise communication and the ability to bring structure to complex topics

  • Full professional fluency in French and English

Why this role is worth taking
This is a high-responsibility role with real visibility, meaningful ownership, and the opportunity to make a tangible difference. You will be trusted, empowered, and expected to use both well.

 

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!

Job Requisition ID:  302869
Location:  Corsier-sur-Vevey
Career Level:  D - Professional (4-9 years)
Working time model:  Full-time

North America Disclosure
The Company is committed to accessibility in its workplaces, including during the job application process. Applicants who may require accommodation during the application process should speak with our Candidate Services team at 844-655-6466 from 8:00am to 5:30pm ET Monday through Friday. If you are a resident of a Connecticut or Colorado, you are eligible to receive additional information about the compensation and benefits, which we will provide upon request.  You may contact 855 444 5678 from 8:00am to 5:30pm ET Monday through Friday, for assistance.

Notice on Fraudulent Job Offers
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