Our client develops, manufactures and distributes cutting-edge surgical technology worldwide.
At its location close to TÜBINGEN, we are currently recruiting for a : REGULATORY AFFAIRS MANAGER (m / f / d)
Homeoffice : 50%
Details : permanent position – 35 hrs. per week – 35 vacation days per year
Aufgaben
- Preparation and updating of technical documentation for medical devices in compliance with MDR 2017 / 745
- Ensuring compliance with applicable regulatory requirements
- Development of test plans, organization of testing procedures, and definition of test characteristics and equipment
- Creation of standard test reports to demonstrate compliance with relevant norms
- Acting as the main contact for notified bodies during technical documentation reviews and regulatory inquiries from development and production teams
- Defining regulatory strategies for the approval of medical devices
Qualifikation
A completed degree in engineering or natural sciencesProfessional experience in Regulatory Affairs for medical devicesKnowledge in the areas of ISO 13485 and MDRExcellent German (C1) and English language skills, both written and spokenStrong coordination and organizational skillsBenefits
What TRIGA Offers You :
New career perspectives and comprehensive consulting for your personal RA careerPositions that match your skills, knowledge, and goalsExclusive job opportunities with background information about the companyOptimization of your application documents and intensive preparation for interviewsDirect access to decision-makers and negotiation of the best compensation packageYOUR CONTACT : Silvio Di Meglio
Managing Director at TRIGA Consulting GmbH & Co. KG
089-8091307-21
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