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Graduate Regulatory Engineer, stoke-on-trent
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Client:
Arevna
Location:
stoke-on-trent, United Kingdom
Job Category:
Other
-
EU work permit required:
Yes
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Job Views:
4
Posted:
04.06.2025
Expiry Date:
19.07.2025
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Job Description:
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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