Regulatory Affairs Specialist (d/w/m)
OttobockLower Saxony, Germany
Posted January 14, 2026
Full Time
About the Company
Ottobock is a leading med-tech company specializing in prosthetics and orthotics. For over 100 years, they have pioneered innovative solutions like the C-Leg microprocessor-controlled leg prosthesis and the C-Brace mechatronic orthosis, helping people regain freedom of movement. With a global network of patient care centers and a focus on digitalization, Ottobock offers customized treatment and cutting-edge products such as wheelchairs and exoskeletons, contributing to stable growth and international presence.
Job Description
The Regulatory Affairs Specialist is responsible for providing relevant documents in a timely manner for various markets in licensing activities, and acting as the first point of contact for various authorities and sales companies for all regulatory issues related to product licensing.
Requirements
- Determination of licensing requirements of international markets and creation of internal strategies for derivation of relevant licensing documents
- Preparation and procurement of regulatory supporting documents
- Correspondence with national and international licensing authorities
- Maintenance and control of product-specific data in SAP for the conformity assessment procedure for medical devices
- Support in the implementation of regulatory requirements in the context of various development projects
Benefits
- Flexible & family-friendly working time models
- 30 days of vacation
- Occupational pension
- Private accident insurance
- Systematic induction program
- Corporate benefits
- Well pass and discounts at local companies
- Controlled room and offers from the health management
- Individual promotion and development
