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:
Join our vibrant team in Vevey as the Site Quality Head! We're seeking a dynamic leader passionate about quality excellence to oversee our Quality Unit, encompassing Quality Assurance, Quality Control, and local Regulatory Compliance for our strategic Biotechnology Drug Substance site. In this influential role, you’ll ensure that all manufactured, controlled, stored, and shipped products meet the highest quality standards. You will uphold current Good Manufacturing Practices (cGMP), Merck Serono Quality Systems, and regulatory requirements, and lead Health Authority and customer inspections. As a key member of the site Leadership team, you’ll shape our operations' future. Embrace this exceptional opportunity to make a lasting impact!
Who You Are:
- University degree in Chemistry, Biology, Pharmacy, or a related field.
- Minimum 10 years of experience in Quality Assurance/Quality Control within the biopharmaceutical industry, preferably in Biotechnology.
- Proven experience with health authority inspections (Swissmedic, EMEA, FDA).
- Strong scientific knowledge in biotechnology and drug substance manufacturing.
- Fluent in both French and English.
- Strong leadership skills focused on team management and development.
- Excellent knowledge of GMP and quality assurance best practices.
- Strategic orientation with strong analytical and problem-solving skills.
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!
and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!
The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.
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