Regulatory Affairs Associate (m/f/d) Regulatory Affairs 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.
Your Tasks Prepare and submit applications to international regulatory authorities for product and change approvalsProvide regulatory inputs to product development projectsDevelop regulatory strategies for changes and new products worldwideLead or coordinate regulatory projects, tasks or compliance initiativesYour Profile University degree, preferably in law, science, or engineeringAt least 1 year of experience in medical device regulatory affairs, ideally with Regulation (EU) 2017/745 and FDA requirementsExcellent written and spoken English (C1 level) requiredBasic German skills (A2 level) requiredStrong team player with high motivation, attention to detail, and reliabilityPlease apply in English and include a cover letter! Further information about MED-EL can be found here.
Your Benefits Central LocationFlexible HoursInternational EnvironmentLanguage CoursesOnboardingWorkplace Well-BeingFurther information Salary will be determined based on professional experience;
the formal minimum salary according to Collective Bargaining Agreement is € 47,810.14. This position is to be filled immediately.If you have any questions please contact Caroline Schenk. Email > About MED-EL MED-ELis 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 3,300 employees around the world. Want to join a company that helps bring the joy of sound to people with hearing loss? Apply now!
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