Our client is a leading manufacturer of high-tech medical solutions for people with various types of hearing loss. With their unique range of state-of-the-art implantable hearing systems, they have helped thousands of people in over 80 countries worldwide to experience hearing and connect with their environment. The company is headquartered in Innsbruck with 22 international subsidiaries and over 800 people working globally.

To support continuing growth in Innsbruck (Austria), they are currently looking for:
 
Regulatory Affairs Spezialist (m/f)
 

Job Description
  • The focal point for development, preparation, and submission of applications and notifications to international regulatory agencies and governing bodies, as assigned.
  • Provides input to product development projects and changes to existing products regarding regulatory requirements and related company requirements.
  • Provides input to the development of regulatory strategies and obtaining regulatory approvals from international regulatory agencies, as required throughout the product life cycle.
  • Reports to Manager, Regulatory Affairs.

Qualification and skills
  • knowledge and demonstrated proficiency in the field of Regulatory Affairs and medical device
  • very good German skills preferred
  • perfect English skills necessary

Interested - working in a challenging and innovative area?!
Please send your application via email using the reference number 22.590 or our online application form.