Job Title: Regulatory Affairs Consultant (MedTech) - Freelance Location: South Germany (20% On-site, 80% Remote)
About the Client: Our client is a leading MedTech company based in the south of Germany, dedicated to advancing healthcare through innovative medical devices. We are currently seeking an experienced Regulatory Affairs Consultant to join our client's team on a 6-month freelance contract. The ideal candidate will have a strong background in regulatory affairs within the MedTech industry and will be responsible for ensuring compliance with all relevant regulations and standards.
Develop and implement regulatory strategies for medical devices.
Ensure compliance with EU MDR, ISO 13485, and other applicable regulations.
Bachelor's degree in Life Sciences, Engineering, or a related field.
Minimum of 5 years of experience in regulatory affairs within the MedTech industry.
Ability to work independently and manage multiple projects simultaneously.
Fluency in English; proficiency in German