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Regulatory Affairs Specialist

Philips ( Best ) +1 andere locaties

Job TitleRegulatory Affairs Specialist Job Description Your role: Develop global regulatory strategies for software medical devices ensuring ongoing compliance throughout the product lifecycle. Prepare and manage regulatory submissions and approvals in the US, Europe, and Canada.

Premium Full-time Medical Device Directive Health Technology Medical Devices MDR External Audit 81.018 EUR

Philips 13 dagen geleden gepost

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