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Senior Regulatory Affairs Engineer
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- Location: Connecticut (Hybrid - 3 days onsite, 2 days remote)
- Our client, a prominent Medical Device manufacturer in Connecticut, is seeking a Senior R&D Engineer specializing in EU MDR Remediation.
- This role involves a hybrid work model, with 3 days onsite and 2 days remote work per week.
- Lead remediation efforts to ensure compliance with EU Medical Device Regulation (EU MDR) standards.
- Generate and maintain documentation related to design control and regulatory compliance.
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