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Senior Manager Quality Systems and Regulatory

 

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

 

You are responsible for regulatory compliance and GMP for the entire manufacturing site.

In these responsibilities, you will be responsible for:

 

- Regulatory compliance

- Inspection readiness of the site

- Internal audit

- System for deviations, CAPA, CCP, documentation, training.

 

You will have a central role for the site and be our contact person for the Merck global organization and for Health Authorities.

For these activities, you will manage a team of around 10 people including experts and associate managers and be part of the quality leadership team.

 

Who you are

 

  • You manage all the quality systems and regulatory compliance with your teams
  • You bring good leadership skills to support your teams in complex projects
  • You have skills to manage Health Authorities inspections
  • You have high knowledge and interest for biotechnology operations
  • You lead by example by adopting irreproachable behavior
  • You guarantee a positive collaboration and team spirit among team members and across departments
  • You encourage good behavior, do not blame human errors and take action against any voluntary violations
  • You foster the identification and sharing of risk situations among the team
  • You amplify the deployment of our site's culture
  • You are fluent in english and french languages
  • You take necessary measures to ensure safety and health of personnel and environmental protection, with the support of EHS


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!

 

Job Requisition ID:  272987
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.

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Job Segment: Quality Manager, CAPA, Environmental Health & Safety, Inspector, Quality, Management, Healthcare

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