Senior Medical Device Regulatory Lead (Onsite) in Leeds

Senior Medical Device Regulatory Lead (Onsite) in Leeds

Leeds Full-Time 63000 - 77000 Β£ / year (est.) Home office (partial)
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At a Glance

  • Tasks: Drive regulatory compliance for medical devices and maintain technical documentation.
  • Company: Medasil Surgical Limited, a leading UK medical device company.
  • Benefits: Flexible working options and opportunities for professional growth.
  • Other info: Join a dynamic team in a supportive environment focused on innovation.
  • Why this job: Make a significant impact in the medical field while ensuring product safety.
  • Qualifications: Experience in regulatory affairs and knowledge of MDR/MDD/UKCA.

The predicted salary is between 63000 - 77000 Β£ per year.

Medasil Surgical Limited, a UK-based medical device company, seeks a Senior Regulatory Affairs Specialist in Leeds to drive regulatory compliance for its product portfolio.

This role is primarily onsite with occasional flexible working.

You will ensure compliance with MDR/MDD/UKCA, maintain Technical Documentation, support registrations with MHRA and EUDAMED, and lead post-market surveillance alignment across the lifecycle.

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Senior Medical Device Regulatory Lead (Onsite) in Leeds employer: MEDASIL SURGICAL LIMITED

Medasil Surgical Limited is an exceptional employer, offering a dynamic work environment in Leeds where innovation meets regulatory excellence. With a strong commitment to employee development, we provide ample growth opportunities and foster a collaborative culture that values each team member's contributions. Our focus on work-life balance, including flexible working options, ensures that you can thrive both professionally and personally while making a meaningful impact in the medical device industry.

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Contact Details:

MEDASIL SURGICAL LIMITED Recruitment Team

We think you need these skills to ace Senior Medical Device Regulatory Lead (Onsite) in Leeds

Regulatory Compliance
MDR/MDD/UKCA Knowledge
Technical Documentation Management
MHRA Registration
EUDAMED Registration
Post-Market Surveillance
Lifecycle Management