Group Manager Regulatory Affairs 100% — Medartis
- Location
- Basel
- Contract
- full-time
- Posted
- 124 days ago
Role overview
We are looking for a Group Manager Regulatory Affairs who will be responsible for our global regulatory strategy, lead a team, ensure compliance with all requirements and drive efficient processes in a dynamic, international environment. Group Manager Regulatory Affairs 100%
- We are looking for a Group Manager Regulatory Affairs who will be responsible for our global regulatory strategy, lead a team, ensure compliance with all requirements and drive efficient processes in a dynamic, international environment. Group Manager Regulatory Affairs 100%
- Your responsibilities
- Professional and disciplinary management as well as further development of a regulatory affairs team
- Degree in Life Sciences, Engineering, Pharmacy or equivalent
- Several years of experience in Regulatory Affairs in the medical technology or pharmaceutical industry
- For the benefit of the patient, Medartis is committed to providing surgeons and surgical staff with the most innovative titanium implants and instruments and providing the best service.
Main responsibilities
- Your responsibilities
- Professional and disciplinary management as well as further development of a regulatory affairs team
- Ensuring compliance with regulatory requirements for the development, manufacture and market introduction of medical devices
- Planning, coordination and control of regulatory activities and projects
- Professional support and advice to the team and internal stakeholders (R&D, quality, production) on regulatory issues
- Responsibility for planning, implementing and monitoring national and international approval procedures (in particular CE marking, FDA)
- Ensuring the quality, consistency and completeness of technical documentation
- Implementation and monitoring of CE conformity assessment procedures
- Management and review of product files (DHF/DHR) and implementation of design reviews
- Assessment of product changes with regard to regulatory requirements and reporting requirements
Key requirements
- Degree in Life Sciences, Engineering, Pharmacy or equivalent
- Several years of experience in Regulatory Affairs in the medical technology or pharmaceutical industry
- Leadership experience and proven experience in leading projects/teams
- Sound knowledge of relevant regulatory requirements
- Experience in technical documentation and approval processes
- Very good German and English language skills in writing and speaking
- Proficient use of MS Office and ideally experience with PLM or document management systems
- Strong organizational skills and a high quality awareness
What the company offers
- For the benefit of the patient, Medartis is committed to providing surgeons and surgical staff with the most innovative titanium implants and instruments and providing the best service.
Application process
- We look forward to your complete online application. Medartis Human resources
Contacts
- T +41 61 633 34 34
- www.medartis.com
Additional details
- We are looking for a Group Manager Regulatory Affairs who will be responsible for our global regulatory strategy, lead a team, ensure compliance with all requirements and drive efficient processes in a dynamic, international environment. Group Manager Regulatory Affairs 100%
- Guidance and support in defining and implementing regulatory strategies Your qualifications
- Structured, solution-oriented and autonomous working method
- We look forward to your complete online application.
Notes and original content
- We are looking for a Group Manager Regulatory Affairs who will be responsible for our global regulatory strategy, lead a team, ensure compliance with all requirements and drive efficient processes in a dynamic, international environment.
- Group Manager Regulatory Affairs 100%
- Guidance and support in defining and implementing regulatory strategies
- Your qualifications
- About Medartis
- Human resources
Questions about this listing
What salary does Medartis offer for this role?
Medartis lists CHF 99'500 - 151'000 gross per year for this position in Basel. This is the salary published in the original listing (or, when the employer omits a figure, a realistic estimate for the role and sector) — the calculator on this site converts it to your actual net take-home once cross-border tax and social contributions are applied.
Is this a full-time role, and what type of contract does Medartis offer?
This listing is a full-time position. The contract type shown here comes directly from the employer's original posting; always confirm exact hours, notice period and probation length with Medartis during the application process, since these details can vary by role even within the same contract category.
Do I need a cross-border work permit for a role in Basel?
EU/EFTA residents living in the border zone of the country adjoining Canton Basel can apply for a G permit; the Swiss employer files it with that canton's migration office after the contract is signed. Border-zone rules and processing times vary by neighbouring country and canton, so confirm the specifics with Basel's cantonal migration office or with HR during the application.
How do I apply for this position at Medartis?
Use the "Apply now" button on this page — it links directly to Medartis's original listing at careers.medartis.com, so your application goes straight to the employer's own applicant-tracking system. Frontaliere Ticino does not collect or forward applications itself.
