Regulatory Affairs Manager

vor 6 Monaten

Zug, Schweiz Viatris Vollzeit

Meda Pharmaceuticals Switzerland GmbH

At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.

Viatris empowers people worldwide to live healthier at every stage of life.

We do so via:
Access - Providing high quality trusted medicines regardless of geography or circumstance;
Leadership - Advancing sustainable operations and innovative solutions to improve patient health; and

Partnership - Leveraging our collective expertise to connect people to products and services.

Key responsibilities for this role include:- Ensuring all activities are performed in compliance with Health Authority requirements and with internal company SOPs- Management of artworks for the relevant portfolio- Interacting with various stakeholders within the Affiliate, the company (Regional or Global RA) and with Authorities in Switzerland (Swissmedic, BAG)- Participate in the review/update of local Regulatory SOPs or Work Instructions

The minimum qualifications for this role are:
- Master’s Degree in Life
- or Pharmaceutical Sciences- 3 years of experience in Regulatory Affairs within the pharmaceutical industry- Knowledge of the national and EU regulations, regulatory guidance, policies, and procedures- Good planning and problem-solving skills, along with the ability to build and manage close relationships with all relevant stakeholders- Fluent in German (written and oral) and good English

What we offer you:
- Friendly working atmosphere in a great team, Great Place to Work® certified- Home office option up to 3 days per week- Development opportunities within an international company

At Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others.

Viatris is an Equal Opportunity Employer.

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