Regulatory Affairs Specialist (m/f/d)

For the Quality and Regulatory Affairs Department of our Tübingen location, we are looking for a

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