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Specialist II, Regulatory Affairs @ Sonova

cityOnsitePart-timePosted 19 days ago

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About this role

Embrace the role of a Regulatory Affairs Specialist II and play a key role in ensuring global compliance for clinical investigations and product approvals. Leverage your expertise in regulatory submissions and medical device regulations to support business growth and regulatory excellence. Grow your career in a dynamic, collaborative environment with opportunities for professional development.. Category: Production / Manufacturing / Repair / Quality Assurance

Skills

regulatory submissionsfda regulationsregulatory complianceeu mdr regulationsproduct registrationregulatory auditsimplantable medical devicestechnical writingstakeholder managementanalytical skillsregulatory risk assessmentregulatory standardssupplier change managementproject supportregulatory agency liaison

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Specialist II, Regulatory Affairs at Sonova | ResuMinder Jobs