Regulatory Affairs Specialist
Kuala Lumpuronsitemid
Posted today · via Workday
About this role
Change people’s lives and love what you do! Cochlear develops world-leading medical devices that help people hear. As a top 100 medical device company and market-leader in implantable hearing devices, more people choose a Cochlear-branded cochlear implant system than any other. Our employees tell us that the number one reason they enjoy working for Cochlear is the opportunity to make a difference to people’s lives. We are currently seeking a Regulatory Affairs Specialist to join our Global Regulatory Affairs team based in Kuala Lumpur. This is an exciting opportunity to partner directly with Product Development and R&D teams, influencing the regulatory strategy of medical devices and software solutions used by thousands of hearing implant recipients worldwide.…
Read the full description on C01 Cochlear Limited (Australia)'s site →
What we'd score you on
reqspace match rubricFive dimensions, recruiter-grade. Upload your resume and we'll generate a written explanation of where you fit and where the gaps are.
1
Skills match
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2
Level fit
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3
Domain experience
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4
Recency
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5
Location fit
This role is based in Kuala Lumpur. We weight your proximity and willingness to relocate.
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