Regulatory and Clinical Affairs Associate
Regulatory and Clinical Affairs Associate
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Not Disclosed
Salary Not Disclosed
1 Vacancy
Job Description
Your mission
- 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 skillsclear 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
Administrative
Place of work: Bern
Preferred start date: by agreement
Workload: 100%
About us
disciplines from cancer treatment to the treatment of hearing disorders.
Required Experience:
IC
Employment Type
Full-Time
