Graduate Engineer

4 days ago


Chelmsford Essex, United Kingdom Arevna Full time

Graduate Regulatory Engineer – Medical Devices
**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. 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. Assist in preparing and submitting regulatory documentation for global approvals (e.g., 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.

A degree in Biomedical Engineering, Mechanical Engineering, or a related discipline.
An interest in regulatory frameworks and quality assurance within the medical device industry.
Prior internship or project experience in the medical device sector is advantageous but not required.

Comprehensive training and mentorship to develop your regulatory expertise.
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.



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