Intern Regulatory Affairs
vor 1 Woche
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.
Every day, we rise to the challenge to make a difference.
As an Intern Regulatory Affairs (M/F/d) you will be gain insight into the different aspects of a Regulatory Affairs Manager function.
Key responsibilities for this role include:
- Staying updated with Swiss regulatory requirements/processes and the authority organization.
- Interacting with various stakeholders within the affiliate, the company (Global Regulatory Affairs, Global Labelling etc.) and the Regulatory Authority
- Ensuring that Regulatory Authority communications with respect to pharmacovigilance and quality are forwarded to PV and QA personnel as required
- Understanding monitoring regulatory trends and strategic input to the management
- Adheres to local processes and procedures to ensure clear regulatory responsibilities within the affiliate in line with Global SOPs and local regulations
The minimum qualifications for this role are:
- You have or are at the end of your Masters studies in Pharmacy, medical or life science area
- Interest and/or first experience in Regulatory Affairs
- Handson mentality, ability to work independently
- Fluent German and English (written and oral)
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.
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