Regulatory Affairs Specialist - Medical Devices

Regulatory Affairs Specialist - Medical Devices

Full-Time 40000 - 50000 Β£ / year (est.) No working from home possible
Newton Colmore

At a Glance

  • Tasks: Lead quality assurance and regulatory affairs for medical devices in a dynamic team.
  • Company: Innovative medical devices company based in Cambridge with a global reach.
  • Benefits: Competitive salary, flexible working hours, and opportunities for professional growth.
  • Other info: Join a forward-thinking company with a commitment to innovation and excellence.
  • Why this job: Make a real difference in healthcare by ensuring the safety and compliance of medical devices.
  • Qualifications: Experience in regulatory affairs or quality assurance, preferably in medical devices.

The predicted salary is between 40000 - 50000 Β£ per year.

Newton Colmore is working with a medical devices company in Cambridge who are looking to hire a regulatory affairs scientist/engineer to join their team. This role will give you an opportunity to take lead on quality assurance and regulatory affairs matters across this international organisation. Although the role will have a focus on medical devices, it will also provide you with experience of new highly regulated industries.

Regulatory Affairs Specialist - Medical Devices employer: Newton Colmore

Join a forward-thinking medical devices company in Cambridge that prioritises employee development and fosters a collaborative work culture. With a strong emphasis on quality assurance and regulatory affairs, you will have the opportunity to lead impactful projects while benefiting from comprehensive training and growth opportunities in a highly regulated industry. The company's commitment to innovation and excellence makes it an exceptional employer for those seeking meaningful and rewarding careers.

Newton Colmore

Contact Details:

Newton Colmore Recruitment Team

We think you need these skills to ace Regulatory Affairs Specialist - Medical Devices

Regulatory Affairs
Quality Assurance
Medical Device Regulations
Compliance Management
Risk Management
Technical Documentation
Project Management