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EnovisEnovis India, India. Full time.

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Regulatory affairsMedical device industry experienceDatabricks WorkflowsContinuous improvementHospitality industry knowledgePatient careTechnical documentationEU Medical Device Regulation (MDR)Change managementCross-functional collaborationProduct developmentCompliance and regulatory requirementsBiomedical EngineeringTime and priority managementWillingness to learn

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