An international MedTech company with headquarters in Berlin is looking for a Regulatory Affairs Professional (m/f/d). You will play a key role in regulatory documentation, MDR compliance, and global product registrations for Class IIb medical devices.
Your responsibilities:
* Prepare and maintain technical documentation (MDR 2017/745)
* Coordinate international product registrations and CE-marking
* Support internal and external audits and CAPA processes
* Collaborate with QA, R&D and Operations departments
Your profile:
* Degree in life sciences, engineering or related field
* 2+ years experience in Regulatory Affairs (preferably in MedTech)
* Excellent knowledge of MDR and ISO 13485
* Strong English skills and a structured mindset
Whatâs offered:
* High-impact role in an innovative, growing company
* Flat hierarchies and direct access to decision-makers
* Hybrid work model, modern office in Berlin
* Competitive salary and development opportunities
Dominik Pichler
Headhunter đ€ Executive Consultant in DACH
Email: [email protected]
Address: NonStop Consulting GmbH | TrogerstraĂe 23 | 81675 MĂŒnchen| Germany
NonStop Consulting GmbH is part of NonStop Consulting S.a.r.l, registered in Luxembourg. Vat Number: 2015 2473 711