Medical Device Regulatory Expert

1 week ago

Melbourne, Victoria, Australia beBeeExpert Full time $130,000 - $170,000
Regulatory Affairs Specialist

Navigate the complex landscape of medical devices and make a real difference in healthcare.

  • Develop and implement regulatory strategies for product development and commercialization.
  • Manage conformity planning, technical documentation, and post-market activities.
  • Provide proactive regulatory guidance to cross-functional teams.

Requirements:

  • 3-5 years of experience in regulatory affairs within the UK and EU markets.
  • A strong ambition and readiness to lead projects.
  • Direct experience compiling technical documentation and managing PMS/PMCF activities.
  • Excellent communication and collaboration skills.
  • A Bachelor's degree or higher in a relevant scientific, engineering, regulatory, legal, or governance discipline.

Benefits:

  • Flexible hybrid working environment.
  • Additional paid day off for your birthday and wellness days.
  • Learn from a world-class team of professionals.
  • Become an owner with shares in the company.

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