Aktuelle Jobs im Zusammenhang mit Intern Regulatory Affairs - Zug - Viatris
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Intern Regulatory Affairs
Vor 5 Tagen
Zug, Schweiz Viatris Vollzeit7087 Mylan Pharma 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...
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Executive Director, Regulatory Affairs
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Senior Expert Regulatory Affairs
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Senior Expert Regulatory Affairs
vor 2 Wochen
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European Regulatory Affairs
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Zug, Schweiz Proclinical VollzeitProclinical are recruiting a European Regulatory Affairs - CTA Liaison for a biotech corporation. This role is on a contract basis and is located in Zug. **Responsibilities**: - Collaborate with regulatory affairs consultants/service suppliers on CTA proposals. - Serve as a representative for EU regulatory affairs at cross-functional study management team...
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Zug, Schweiz NonStop Consulting VollzeitJoin a Leading Regulatory Affairs Team! About Our Client With a diverse portfolio of iconic brands across 20 countries, our client operates in Australia & New Zealand, Asia, and Africa. Their team is dedicated to putting people’s health first every day, and they pride themselves on their unique blend of leadership and empowerment. Our client, celebrated as...
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Senior Expert Regulatory Affairs
vor 2 Wochen
Zug, Schweiz gloor&lang AG VollzeitShape CMC regulatory strategy for complex biologics in a fast-growing biotech environment For a fast-growing, internationally active biotech company focused on biosimilar development, we are currently looking for a Senior Expert Regulatory Affairs with a strong CMC focus. Workplace is Region Zug-Zurich in Switzerland, 3d office required. This is a key role...
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Senior Expert Regulatory Affairs
Vor 7 Tagen
Zug, Schweiz gloor&lang AG VollzeitShape CMC regulatory strategy for complex biologics in a fast-growing biotech environment For a fast-growing, internationally active biotech company focused on biosimilar development, we are currently looking for a Senior Expert Regulatory Affairs with a strong CMC focus. Workplace is Region Zug-Zurich in Switzerland, 3d office required.This is a key role...
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Head of Regulatory Affairs, Europe
Vor 6 Tagen
Zug, Zug, Schweiz Scholar Rock VollzeitScholar Rock is a biopharmaceutical company that discovers, develops, and delivers life-changing therapies for people with serious diseases that have high unmet need. As a global leader in the biology of the transforming growth factor beta (TGFβ) superfamily of cell proteins and named for the visual resemblance of a scholar rock to protein structures, the...
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Regulatory Affairs Manager
vor 9 Stunden
Zug, Schweiz Proclinical VollzeitProclinical are recruiting a Regulatory Affairs Manager for a biotech corporation. This role is on a contract basis with the ability to work remotely in Europe. **Responsibilities**: - Handle the relationship with the Clinical Research Organisation contracted for some clinical studies. - You will assist with different regulatory proposals to the marketing...
Intern Regulatory Affairs
vor 2 Wochen
Viatris Pharma 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.
Every day, we rise to the challenge to make a difference. As a Regulatory Intern (M/F/d), Strategy and Policy, Europe you will be responsible for developing an oversight of Regulatory Strategy and Policy activities across Europe.
Key responsibilities for this role include:
- Supporting the team with Policy Paper and Legislation reviews- Assisting to collect the feedback to any surveys / requests for information from Health Authorities / Medicines for Europe (MfE) / National Trade Associations / Internal Stakeholders- Providing support with Regulatory Intelligence and Competitive Intelligence activities- Assist with Marketing Authorization Applications’ Performance review for all pending and completed Viatris’ group procedures- Assist Line Manager by supporting departmental initiatives as may be required.- Develop an awareness of regulatory requirements (including legislation, guidelines, industry best practice, and liaison with Competent Authorities) and use this information to optimise departmental procedures and processes and to ensure Health Authority requirements and Regulatory Compliance are maintained
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- Excellent IT skills with proficiency in MS Office (Excel, Word and PowerPoint), experience in working with databases and document management systems is a plus- Previous experience in Regulatory Affairs considered an advantage- Interest in Regulatory Strategy and Policy- Fluent in English (written & oral) is mandatory
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.
