At a Glance
- Tasks: Lead UKCA and UK MDR regulatory activities for medical devices and provide expert guidance.
- Company: Join TÜV SÜD Group, a leader in regulatory affairs and compliance.
- Benefits: Competitive salary, professional development, and a supportive work environment.
- Other info: Opportunity to grow in a dynamic and impactful field.
- Why this job: Make a real difference in the medical device industry with your expertise.
- Qualifications: Degree in science/engineering and five years of regulatory experience required.
The predicted salary is between 50000 - 65000 £ per year.
TÜV SÜD Group is seeking a Regulatory Affairs professional to lead UKCA and UK MDR regulatory activities for medical devices.
You will review regulations, support training, and provide regulatory guidance while coordinating CAPA and audit responses.
The role requires a university degree in a science/engineering field and at least five years of medical device regulatory experience with UKMDR and EU MDR/IVDR, plus excellent English communication skills.
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UKCA Regulatory Compliance Specialist employer: TUV SUD Limited
At TÜV SÜD Group, we pride ourselves on fostering a dynamic and inclusive work environment where innovation thrives. As a Marketing Business Partner in the UK & Nordics, you will have the opportunity to shape impactful marketing strategies while collaborating with diverse teams across more than 100 countries. We are committed to your professional growth, offering comprehensive training and development opportunities that empower you to excel in your career and contribute meaningfully to our mission of ensuring safety and progress in technology.
