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 Erbe medical devices marketed 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:
- Flexible working hours
- Induction programme and on-demand training
- Family-friendly work environment
- Occupational health and safety management
- Occupational pension plan
- Secure job in a modern company
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 mail to career@erbe-med.com.