For the Quality and Regulatory Affairs Department of our Tübingen location, we are looking for a
Regulatory Affairs Specialist (m/f/d)
Your Responsibilities
- Conduct and support official registrations and approvals for all medical devices placed on the market by Erbe from outside the EU
- Collaborate with distribution partners, service providers and authorities
- Evaluate requirements for international approvals and review and prepare regulatory documentation in collaboration with the company's specialist departments
- Coordinate regulatory projects, ensuring adherence to deadlines and schedules
Your Skills
- University degree and initial professional experience in the field of international medical device approvals
- Good understanding of technology and complex interrelationships
- Interest in working with international legal requirements and regulations
- Good problem-solving and communication skills
- Intercultural competence and very good command of spoken and written English
Benefits:
- Ergonomic workstations with state-of-the-art equipment
- Extensive local canteen offering with breakfast, lunch and complimentary beverages (water, coffee)
- Good work-life balance with support for holiday childcare and external counselling services for any situation
- Attractive monthly salary with collectively agreed and non-collectively agreed special payments (Christmas bonus, holiday bonus, etc.)
- Working time account for some flexibility in working hours and the possibility of hybrid work
- Extensive internal and external training opportunities as well as support for further and continuing education
- A job in a family-owned business in a crisis-proof industry
Are you interested?
If so, we look forward to receiving your application, including your salary expectations and the earliest possible starting date. Please apply via our career portal.