RA Specialist

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Job Detail

  • Job ID 538614

Job Description

Are you passionate about driving innovation and ensuring patient safety in the MedTech industry? A leading global medical device manufacturer is looking for a Regulatory Affairs Specialist to support international registration processes and product development for Class IIa and IIb devices in the Vascular Intervention space.Key Details:

  • Start Date: ASAP
  • Contract Duration: 6 months
  • Location: Zurich, Switzerland (Onsite/Hybrid)
  • Languages: English required
  • Interviews: Flexible & fast process

What you’ll be doing:

  • Managing regulatory submissions and lifecycle activities across the EU, US, Japan, and other key markets
  • Providing strategic regulatory input during product development
  • Preparing responses to authorities and notified bodies
  • Maintaining up-to-date documentation and internal procedures for compliance

What we’re looking for:

  • Degree in a scientific or technical field (natural sciences, pharmacy, pharmacology, medicine, or engineering)

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