Posted in: Other in Utrecht | Posted: |
- Responsible for the product groups, RA assessments of product changes and maintenance of technical documentation
- Supporting sales regarding registration of the products in several countries
Description
- Create and keep up-to-date the regulatory compliance of the product portfolio
- Support R&D projects and product changes on RA matters
- Keep technical documentation regarding the product portfolio up-to-date
- Examine product conformity and guide the conformity assessment process
- Provide technical and RA expertise related to approval of medical devices and technical documentation
- Realise global registration of all products within the portfolio
- Keeping up-to-date the knowledge of RA regarding medical devices and MDR
- Stay informed regarding relevant regulatory changes in legislation and guidelines and communicate them proactively
Job Offer
- Salary between 50-80K
- Individual performance and Company performance based bonus
- Pension plan with Nationale Nederlanden
- Travel reimbursement
- 25 Holidays
- Hybrid role (40% in the office)
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