Stettler Consulting AG
St. Gallen
Head of Regulatory Affairs & QM (m/f)
- 12 October 2026
- 100%
- Permanent position
- German (Fluent), English (Fluent)
Skills
BiomedizinKommunikationMedizintechnikPharmazieRegulatory AffairsStrategieunternehmerischZulassung von MedizinproduktenAbout the job
Our client is a renowned Swiss family business with an international focus. It is committed to improving the quality of life for people in certain medical indication areas with high-quality and innovative offerings. On their behalf, we are looking for a leader with several years of experience in Regulatory Affairs in the medical/medical technology environment. Region: Eastern Switzerland / Industry MedTech.
What you can look forward to:
- Healthy Swiss traditional company with global reach
- Highly versatile and strategic role with a lot of personal responsibility and scope for design
- Attractive employer and manufacturer of an innovative product portfolio
Your responsibilities and tasks:
- Professional and personnel management as well as further development of the local Regulatory Affairs team and co-design of the global Regulatory Affairs strategy
- Ensuring regulatory compliance throughout the entire product lifecycle
- Development of regulatory strategies for new products, product changes and lifecycle management including technical and regulatory documentation as well as responsibility for quality management
- Responsibility for international product registrations and market approvals
- Close cooperation with R&D, quality assurance, operations, marketing and sales departments
- Representation of the company towards notified bodies, authorities and international regulatory institutions
- Support of internal and external audits, inspections as well as continuous optimisation of regulatory processes and systems (ISO 13485)
Your profile:
- Completed studies in natural sciences, medical technology, biomedicine, pharmacy etc.
- Several years of professional experience in Regulatory Affairs for medical devices
- Sound knowledge of the EU Medical Device Regulation (MDR 2017/745) is a prerequisite
- Experience in managing complex international approval and registration projects
- Strategic thinking and entrepreneurial action as well as solution-oriented working style
- Strong communication skills and fluent in German and English
Contact
Call us or send us your application documents quoting the reference number JB-202. Roger Stettler looks forward to meeting you in person.