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)
