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RA Specialist

Zurich • Panda International

23 dagen geleden

RA Specialist Zurich • Panda International

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Gevraagd

37 - 40 uur
Engels (taal)

Aanbod

Vast contract

Vacature in het kort

Zurich

Do you have a passion for innovation and patient safety in MedTech? A top medical device company seeks a Regulatory Affairs Specialist to aid in global registration and development of Class IIa and IIb Vascular Intervention devices. You'll manage regulatory submissions in key markets and provide strategic input during product development. Enjoy a flexible interview process and the chance to work onsite or hybrid in Zurich. Join a dynamic team and make a difference in the medical field. Explore further to see the impact you could make.

Over het bedrijf

Panda International

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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

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