Graduate Regulatory Engineer

1 week ago

Chelmsford, United Kingdom Arevna Full time

Graduate Regulatory Engineer – Medical Devices


**Must hold full right to work, no sponsorship available**


On-site 5 days/week in Chelmsford - Relocation allowance available


Are you a recent graduate looking to start your career in the exciting world of medical devices? My client, an innovative leader in the medical technology industry, is seeking a Graduate Regulatory Engineer to join their growing team. This is a fantastic opportunity to gain hands-on experience in a highly regulated and rewarding sector while contributing to life-changing healthcare solutions.


About the Role:

As a Graduate Regulatory Engineer, you’ll play a key role in ensuring compliance with global regulatory standards while supporting the development of cutting-edge medical devices. You’ll work closely with experienced professionals and cross-functional teams to bring innovative products to market safely and efficiently.

Key Responsibilities:

  • Assist in preparing and submitting regulatory documentation for global approvals (e.g., 510(k), CE marking).
  • Support the development and maintenance of Quality Management Systems (QMS) compliant with ISO 13485 and FDA regulations.
  • Contribute to risk management activities, including dFMEA and pFMEA processes.
  • Review and maintain documentation to ensure regulatory and quality standards are met throughout the product lifecycle.
  • Collaborate with R&D, quality assurance, and manufacturing teams on compliance and process improvements.


What We’re Looking For:

  • A degree in Biomedical Engineering, Mechanical Engineering, or a related discipline.
  • Strong attention to detail and excellent problem-solving skills.
  • An interest in regulatory frameworks and quality assurance within the medical device industry.
  • Strong communication skills and a collaborative attitude.
  • Prior internship or project experience in the medical device sector is advantageous but not required.


What’s on Offer:

  • Comprehensive training and mentorship to develop your regulatory expertise.
  • A supportive, collaborative team environment.
  • The chance to work on innovative products that improve patient outcomes.
  • A clear pathway for career growth within the medical device industry.


This is an incredible opportunity to launch your career with a company that values innovation, quality, and improving lives.


If you’re interested, please apply or get in touch with me directly for more details. Don’t miss this chance to join a pioneering organization and make a real impact in healthcare

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