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Senior Specialist, International Regulatory Affairs @ Sonova

cityOnsitePart-time
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About this role

Join our team as a Senior Specialist, International Regulatory Affairs and play a key role in global regulatory activities for Class III medical devices. Drive approvals, support product development, and ensure compliance across international markets. If you have strong regulatory expertise and thrive in a dynamic environment, we want to hear from you!. Category: Production / Manufacturing / Repair / Quality Assurance

Skills

regulatory submissionsglobal regulatory compliancemedical device regulatory affairsproduct change assessmentregulatory strategyregulatory strategy and guidancedocumentation preparationregulatory impact assessmentregulatory affairs proceduresregulatory information management systemsagile plmsapmicrosoft officedata managementstakeholder management

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