Offer summary
Qualifications:
Technical/science degree or equivalent, 2-4 years in regulatory medical device development, Knowledge of ISO 13485, ISO 27001, MDR, Innovative and analytical mindset, Fluent in German and English.Key responsabilities:
- Develop regulatory strategies for products
- Prepare documentation for regulatory compliance
- Maintain and optimize management systems
- Prepare and conduct audits/inspections
- Collaborate with cross-functional teams