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Graduate Regulatory Affairs Associate – Medical Devices

Graduate Talent
Posted 8 hours ago, valid for a month
Location

Leamington Spa, Warwickshire CV311JX, England

Salary

£27,000 - £32,000 per annum

Contract type

Full Time

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Sonic Summary

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  • Join a market-leading healthcare company with over 40 years of global experience that manufactures high-quality medical devices in the UK and supplies products to over 70 countries.
  • As a Graduate Regulatory Affairs Associate, you will support compliance for medical devices, ensuring they meet international regulations, while gaining hands-on experience in the life sciences industry.
  • The role requires a graduate in Biomedical Engineering, Biochemistry, Life Sciences, or a related discipline, along with strong attention to detail and communication skills.
  • A full UK driving licence is necessary for occasional travel, and the position offers a competitive salary with structured training and mentoring in Medical Regulatory Affairs.
  • This opportunity provides exposure to global compliance frameworks and career progression within a supportive and friendly team.

Join a market-leading healthcare company with over 40 years of global experience. Our client manufactures high-quality medical devices in the UK and supply products to over 70 countries.

This is a fantastic opportunity to start your career in a specialist field within the life sciences industryand gainhands-on experience in a growing SME, learning the business from the bottom up

The Role:

As a Graduate Regulatory Affairs Associate, you will support the compliance of our medical device portfolio with international regulations

Responsibilities include:

  • Compliance assurance

Ensuring that medical devices meet all legal requirements before they are sold

  • Product development support

Guiding the development and lifecycle management of new and existing medical devices to ensure they meet regulatory standards

  • Market surveillance

Monitoring the performance and safety of devices already on the market and reporting any issues to the appropriate regulatory body

  • Documentation and submissions

Preparing and submitting required documentation to regulatory agencies for approval

  • Risk assessment

Analysing and managing the risks associated with medical devices to ensure patient safety

  • Liaising with authorities such as the MHRA

Communicating with regulatory bodies, such as MHRA, to provide information and address concerns

While primarily office-based, the role involves occasional travel to manufacturing sites and trade shows, so a full UK driving licence is required.

Requirements:

  • Graduate in Biomedical Engineering, Biochemistry, Life Sciences, or a related discipline
  • Strong attention to detail, communication, and analytical skills
  • Excellent communication skills
  • An understanding of regulatory affairs
  • Right to work in the UK (sponsorship not provided)

What We Offer:

  • Competitive salary
  • Structured training and mentoring in Medical Regulatory Affairs
  • Supportive and Friendly Team
  • Exposure to global compliance frameworks and career progression opportunities
  • Free on-site parking, early finish at 2:30pm Fridays, company pension scheme

Apply now in a few quick clicks

By applying, a CV-Library account will be created for you. CV-Library's Terms & Conditions and Privacy Policy will apply.

SonicJobs' Terms & Conditions and Privacy Policy also apply.