Regulatory Affairs Associate, Global Registrations (m / f / d)

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 3,000 employees around the world.

RA_12507

Regulatory Affairs Associate, Global Registrations (m / f / d)

Regulatory Affairs

Innsbruck, Austria

Professionals Full-Time 38.5h 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.

• Compilation and international submissions of regulatory dossiers
• Development of regulatory assessments and submission strategies
• Gathering of regulatory intelligence with focus on communicating with MED-EL's areas / subsidiaries
• Management of informational lists and databases
• Coordination and communication with sales
• Higher degree and / or experience preferably in a legal, science or engineering discipline, with a health science or biomedical component e.g. HTA, public health, clinical research, regulatory affairs
• Written and verbal fluency in English; and other languages beneficial
• Proficient using PC and MS applications software
• Attention to detail and excellent organizational skills
• Strong orientation to teamwork and accomplishment of goals
• Central Location
• Employee Discounts
• Flexible Hours
• Further Training
• International Environment
• 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.