ExpertiseUpdated on 23 February 2026
Regulatory Affairs and Quality Management Support Medtech
About
Qualitymanagement and Regulatory Affairs Services for Medical Devices, Medical Device Software, In Vitro Diagonstic Devices and Combination Products. Cybersecurity Quality Management and Regulatory Affairs.
Safety and (Cyber) Security Risk Management, Software Safety and Cybersecurity, Data Protection, E2E Software Lifecycle Process (IEC 62304), Computer System Validation (CSV), Documentation and Submission of Medical Device Software.
Usability Engineering and Management, Interdisciplinary Project Management, Remediation Project Management, Product Lifecycle Management, Software- and Hardware Lifecycle Management, Requirements Engineering and Management, Configuration and Change Management, CAPA Management, Manufacturing Process (Production) Management, Platform Engineering and Management, Waste Management
Similar opportunities
Expertise
- Other
- Healthcare
- Biotech, Pharma and Cosmetics
- Industrial Equipment and Machinery
Bernhard Bichsel
Co-CEO at ISS AG, Integrated Scientific Services
Bern, Switzerland
Project cooperation
From Scientific Discovery to Market-Ready MedTech
Stefano Brianza
Owner at Biomech Innovations AG
Nidau, Switzerland
Expertise
Clinical Operations & Project Manager/Clinical Trial & Data Manager
- Healthcare
- Biotech, Pharma and Cosmetics
Madhuparna Ganguly
Clinical Operations & Project Manager | MBA @ SwissTPH | Clinical Research Scientist - QA & RA at University of Geneva
Zurich, Switzerland