Jobbeschreibung
MED-EL is a leading manufacturer of innovative medical devices for the treatment of various types and degrees of hearing loss. Our unique portfolio of implantable hearing solutions benefits thousands of individuals in more than 140 countries worldwide. With headquarters in Innsbruck, Austria, MED-EL has over 2,800 employees around the world.
RA_32502
Regulatory Affairs Specialist (m/f/d)
Regulatory Affairs
Innsbruck, Austria
Professionals Full-Time 38.5 h Permanent
Our Regulatory Affairs department ensures that products comply with applicable regulations and standards. This includes providing strategic input to product developments, obtaining and maintaining product registrations and approvals, communicating with authorities, and monitoring regulatory changes to ensure continued compliance.
- Prepare and submit applications to international regulatory authorities for product and change approvals
- Provide regulatory inputs to product development projects
- Develop regulatory strategies for changes and new products worldwide
- Lead or coordinate regulatory projects, tasks or compliance initiatives
- University degree, preferably in a legal, science or engineering discipline
- Previous medical device regulatory experience is preferred
- Excellent spoken and written English is required, German proficiency is an advantage
- Team player, highly motivated, attention to detail and dependable
- Central Location
- Employee Discounts
- Flexible Hours
- International Environment
- Onboarding
- Workplace Well-Being
Minimum Salary
Salary will be determined based on professional experience; the formal minimum salary according to Collective Bargaining Agreement is € 46,781.00.