Regulatory Affairs Expert (Medical Devices) till Sunmedic AB
Sunmedic AB · Vellinge, Sverige
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- Firma
- Sunmedic AB
- Plaz
- Vellinge, Sverige
- Aart vum Kontrakt
- Vollzäit
- Publizéiert den
- 19. Juni 2026
Iwwer dës Plaz
1) About the job Sunmedic is a forward-thinking medical device company dedicated to delivering innovative, safe, and effective products for patients. We are seeking a motivated Regulatory Affairs Expert to join our team and help ensure our products meet all regulatory requirements across markets. This role offers the opportunity to influence global regulatory strategies, collaborate with cross-functional teams, and contribute to bringing life-saving devices to patients. 2) What you will do - Develop and implement regulatory strategies for medical device products across markets, with a focus on MDR compliance. - Prepare, assemble, and submit regulatory documentation (technical files, PMCF/PSUR where applicable, EU MDR/UK MDR, 510(k) for the US, etc.) and manage lifecycle activities. - Monit…
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