Your mission
Your Mission: You will play a key supporting role in the development and upkeep of regulatory documentation to ensure compliance with global standards. Key tasks include:
- Support the creation, submission, and maintenance of regulatory documentation
- Liaise with Research & Development to create and maintain technical files
- Monitor regulatory requirements and help integrate them into product development
- Assist with literature reviews and preparation of clinical evaluation reports
- Contribute to the development and improvement of department procedures
Your profile
- Educational background in Engineering
- Strong English writing skills—clear, structured, and concise
- Proficient in MS Word and other information management tools
- Interest in learning and understanding medical device regulations (prior knowledge is a plus)
- Any experience in Regulatory Affairs or in the field of surgical navigation / robotics is a plus
You are
- A curious, fast learner eager to develop in the medical technology field
- A reliable, collaborative team player who enjoys working across functions, adapts to changing priorities, and follows through on commitments
- Detail-oriented and organized, with excellent problem-solving skills
- Open, adaptable, and motivated to contribute in a dynamic environment
Why us?
We offer a challenging role in a multinational, innovative, fast-growing, and dynamic environment. In our company you can create, shape, and take on responsibility. Our unique company culture is shaped by our passion and values.
Administrative
We look forward to receiving your application with CV, letter of motivation, diploma (must), and references (optional). (Applications from recruiters will not be considered). For questions, please contact Mr. Augustin Blazevic (+41 31 306 26 05).
Place of work: Bern
Preferred start date: by agreement
Workload: 100%