Senior Regulatory Affairs Specialist

5 days ago


Gothenburg, Västra Götaland, Sweden Randstad Full time

We are seeking a highly motivated and experienced Mid-Senior Quality Assurance/Regulatory Affairs (QA/RA) Specialist to join our dynamic and rapidly growing MedTech company.

This role offers an exciting opportunity to contribute to the development of cutting-edge products while ensuring compliance with the highest industry standards in medical devices.

Main Responsibilities
  • Oversight of quality assurance processes and regulatory requirements for medical devices.
  • Cross-functional collaboration with R&D, manufacturing, and product management teams.
  • Development, implementation, and improvement of quality systems and regulatory strategies.
Key Qualifications
  • University degree in life science, engineering, or other relevant area.
  • Comprehensive experience (+5 years) of both operational and strategic responsibility for QA and RA in the medical device industry.
  • In-depth knowledge and experience in registering products in different markets globally.
  • Familiarity with relevant regulations; MDR and 21CFR Part 820, ISO 13485, and other international standards and guidelines.


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