Global Regulatory Affairs Specialist (MedTech, SaMD)
Cochlear
- Hybrid
About this role
Summary from our partner feed — apply on the employer site for the full posting.
Cochlear in Kuala Lumpur is seeking a Regulatory Affairs Specialist to partner with Product Development and R&D, shaping regulatory strategy for medical devices and software solutions used globally. You will work with global teams to ensure submissions readiness and lifecycle management from concept through commercialization.
The role emphasizes cross-functional collaboration, regulatory intelligence, and ensuring compliance across US, EU and APAC markets within a hybrid Malaysian work model. #J-18808-Ljbffr. Compensation: 120 - 180.
At a glance
- Employer
- Cochlear
- Location
- Kuala Lumpur
- Compensation
- MYR 120 – MYR 180
- Posted
- Yesterday
- Source
- en-my.whatjobs.com
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