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Regulatory Affairs Associate

Omega Resource Group
Posted 3 days ago, valid for 6 days
Location

Gloucester, Gloucestershire GL11AP, England

Salary

£35,000 - £42,000 per year

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Contract type

Full Time

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Sonic Summary

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  • The position of Regulatory Affairs Associate is located in Gloucester and is a permanent, onsite (hybrid) role.
  • The key responsibilities include maintaining regulatory compliance, organizing technical documentation, and supporting international registrations.
  • Candidates should have proven experience in a medical device regulatory or quality role and a solid understanding of regulatory processes, particularly ISO 13485 and MDR.
  • Internal QMS auditing experience and the ability to prioritize and meet deadlines in a regulated environment are also required.
  • The salary for this position is competitive, though specific figures are not provided, and candidates should have relevant experience in regulatory affairs.

Position: Regulatory Affairs Associate
Location: Gloucester
Job Type: Permanent / Onsite (Hybrid)

Our client, a global leading manufacturing business based in Gloucester are on the hunt for a detailed and organised Regulatory Affairs Associate!

Role and Responsibilities – Regulatory Affairs Associate
In this role, your key responsibility is to maintain regulatory compliance, obligations to international regulations and organisation of related technical documentation.

Other responsibilities include:

  • Ensure documentation aligns with ISO 13485, ISO 14971 and where applicable IEC (phone number removed)
  • Support preparation, review, and maintenance of Technical Documentation, including device description, GSPR, risk management, clinical evaluation, PMS, PMCF, and labelling.
  • Partner with R&I, Engineering, Quality, Manufacturing, Sales and Supply Chain to ensure regulatory deliverables are embedded and on time
  • Support international registrations (e.g., FDA listing support, Canada, Australia) as business needs evolve.

Experience or Qualifications – Regulatory Affairs Associate

  • Proven experience in a medical device regulatory / quality role
  • Sounds understanding of regulatory processes within med devices standards (ISO 13485, MDR, FDA 21 CFR Part 280)
  • Internal QMS auditing experience
  • Ability to prioritise and deliver to deadlines in a regulated environment.

Candidates who currently are a Regulatory Affairs Associate, Regulatory Affairs Engineer, Regulatory Affairs Specialist or Quality & Regulatory Associate may be suitable for this position.

For more information regarding this Regulatory Affairs Associate role please contact Ben Herd on (phone number removed) or (url removed)

Omega Resource Group is acting as an Employment Agency in relation to this vacancy.

Omega Resource Group is an employment agency specialising in opportunities at all levels within the Engineering, Aerospace, Automotive, Electronics, Defence, Scientific, Oil & Gas, Construction and Manufacturing sectors.

For details of other opportunities available within your chosen field please visit our website (url removed)

Omega is an employment agency specialising in opportunities at all levels within the Engineering, Manufacturing, Aerospace, Automotive, Electronics, Defence, Scientific, Energy & Renewables and Tech sectors.

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