Regulatory Affairs Specialist

Cochlear

Kuala Lumpur, Malaysia
Regulatory support for medical devices
Experience in product development
Strong organizational skills
Cochlear develops world-leading medical devices that help people hear

Job Summary

  • Cochlear develops world-leading medical devices that help people hear.
  • The Regulatory Affairs Specialist provides regulatory support across the lifecycle of Cochlear products.
  • Employees enjoy the opportunity to make a difference to people’s lives.

Matching Summary

Cochlear develops world-leading medical devices that help people hear.

Skills & Requirements

Must-have

  • Regulatory support for medical devices
  • Experience in product development
  • Strong organizational skills

Nice-to-have

  • Advanced degree or RACS certification
  • Experience in medical device development
  • Strong analytical abilities

Key Requirements

  • Bachelor’s degree in biomedical engineering
  • 3+ years’ experience in regulatory affairs
  • Working knowledge of global medical device regulations

Work Rights

Not specified

Tailored Resume

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