Regulatory Affairs Associate – Medical Device Belgium
Full Time
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What to Expect
- Conduct regulatory impact assessments for product changes, including determination of letter-to-file versus submission requirements.
- Manage annual registrations, license renewals, and ongoing regulatory notifications.
- Support the preparation, submission, and maintenance of FDA dossiers and related technical documentation.
- Coordinate the collection, review, and consolidation of data for international regulatory registrations.
- Collaborate with global Regulatory Affairs partners and cross-functional stakeholders to ensure timely, compliant submissions.
- Execute administrative, documentation, and procedural activities supporting the Regulatory Affairs function.
Requirements
- Bachelor degree
- Min 4 years of experience in Regulatory Affairs in the medical device
- Proven experience with global submissions, preferably including FDA,
- Excellent communication and problem-solving skills
- Fluent in English (written and spoken).
If you have difficulty in applying, have any questions or you cannot find what you are looking for please contact us on 0044 (0) 207 421 0000 or email [email protected]
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