At a Glance
- Tasks: Ensure compliance with UKCA regulations and lead global regulatory initiatives.
- Company: Join TÜV SÜD UK, a leader in regulatory affairs.
- Benefits: Competitive salary, professional development, and a supportive work environment.
- Other info: Opportunity to collaborate with global teams and drive impactful change.
- Why this job: Make a difference in medical device regulation on a global scale.
- Qualifications: Five years in medical device regulation and strong communication skills.
The predicted salary is between 50000 - 65000 £ per year.
TÜV SÜD UK is seeking a regulatory specialist to ensure procedural compliance of UKCA conformity assessment activities with UKCA requirements and internal QMS.
You will collaborate with Global Regulatory colleagues, lead on authority-led requests and drive CAPA activities within a global framework.
Applicants should have a minimum of five years in medical device regulation with UKMDR/EU MDR/IVDR, strong communication skills, and the ability to present at audits and training sessions.
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UKCA & Global Regulatory Affairs Specialist in Fareham employer: TÜV SÜD
TÜV SÜD is an exceptional employer that fosters a culture of innovation and excellence, particularly in the Defence and Aerospace sectors. Located in Fareham, our team enjoys a competitive salary, generous holiday entitlement, and comprehensive wellbeing support, all while working with cutting-edge technologies in a collaborative environment. We prioritise employee growth and inclusivity, ensuring that every team member feels valued and empowered to contribute to meaningful projects that impact society.
