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Medical Device Regulatory Affairs Associate

4 months ago

Yeadon, United Kingdom Xiros Full time

We are looking for a Science or Engineering graduate to join our small Regulatory team based in Yeadon, Leeds as a Regulatory Affairs Associate to ensure that our textile-based, orthopaedic, implantable medical devices can continue to be sold throughout the world.

The role:

  • Support with generating Technical Files and Device Master Records for newly registered devices.
  • Perform Risk Management file reviews and updates for approved devices.
  • Perform reviews of documents for other departments in the company.
  • Support with day to day regulatory and administrative tasks, i.e., maintenance of Medboard, MHRA site, BSOL, standard reviews etc.,

Essential Requirements:

  • It is an industry requirement that you hold a degree in Science or Engineering. Please do not apply if you do not have such a degree, as this is non-negotiable.
  • You must be a self-starter, proactive, driven and well organised with good administrative skills.

Desirable Requirements:

  • Previous experience in a Regulatory or Quality Affairs role within medical devices would be advantageous.
  • Experience in supporting distributor approval in a medical device company would also be beneficial.
  • Experience in writing and reviewing Technical Files.
  • Experience of new product registration in the USA (510k) and EU (CE marking).


Starting salary £33,250 p.a. with opportunity for progression. Excellent range of core and flexible benefits including non-contributory S.I.P.P; cash plan; opportunity for private medical insurance, gym membership, Metro-card; enhanced holiday allowance; subsidised lunches; free drinks and fruit; wellness programme; free and subsidised sports and social events; company parties; flexi-time; opportunity to work on site three days per week and remotely two days per week; ongoing training and development.