Graduate Regulatory Engineer

JR United Kingdom; Basildon; On-site; GBP 25,000 - 35,000; Full time

Job summary

A leading company in the medical technology industry is looking for a Graduate Regulatory Engineer to ensure compliance with global regulations and support innovative medical devices. This role provides comprehensive training and a clear career growth pathway in a collaborative environment focused on improving patient outcomes.

Benefits

Comprehensive training and mentorship

Supportive team environment

Pathway for career growth

Qualifications

• Relevant degree in Biomedical or Mechanical Engineering required.
• Strong attention to detail and problem-solving skills.
• Interest in regulatory frameworks and quality assurance.

Responsibilities

• Assist in preparing and submitting regulatory documentation for global approvals.
• Support development and maintenance of Quality Management Systems compliant with relevant regulations.
• Contribute to risk management activities, including dFMEA and pFMEA.

Skills

Attention to Detail

Problem Solving

Communication

Education

Degree in Biomedical Engineering

Degree in Mechanical Engineering

Degree in a Related Discipline

Job description

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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!