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)
- Initial experience in regulatory affairs for medical devices
- Solid knowledge of MDR and international regulations
- Proficiency in Microsoft Office (SAP is a plus)
- Fluent in English; additional languages (e.g., German) are a plus
Apply below ASAP
Interviews happening next week