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  • Job type

    Permanent
  • Location

    Leeds
  • Working Pattern

    Full-time
  • Specialism

    Regulatory Affairs
  • Industry

    Scientific and R&D
  • Pay

    £30,000 - £35,000

Regulatory Compliance | Medical Devices | Full-Time | Hybrid

Our client is a global leader of Medical Device products and has decades of experience working within various markets. This is the ideal opportunity for someone who is passionate about Regulatory Compliance and has excellent written and verbal skills.


Key responsibilities:
  • 1–3 years of experience in Medical Devices.
  • Experience with regulatory labelling requirements for Medical Devices.
  • Able to establish and maintain documents for current global market clearance/registration status.
  • Experience working within multi-functional project teams, external manufacturers, and regulatory authorities.

Benefits:
  • Bonus scheme.
  • Hybrid working (5 days on-site a fortnight).
  • Flexible working hours.
  • 25 days holiday + Bank Holidays (Lunchtime finishes the day before a bank holiday).
  • And a lot more...

If this sounds of interest to you, please submit your CV and a consultant will be in touch.
Please note that sponsorship cannot be offered at this time.

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