Product Development Engineer

JR United Kingdom; Bury St Edmunds; On-site; GBP 40,000 - 80,000; Full time

Job summary

An innovative company at the forefront of healthcare technology is seeking a passionate Product Development Engineer. This role offers the opportunity to drive product development projects for advanced medical devices, collaborating with diverse teams to ensure successful delivery. Candidates will leverage their engineering expertise to develop prototypes, conduct testing, and maintain essential design documentation. If you are eager to contribute to life-changing medical technology and thrive in a dynamic environment, this is the perfect opportunity for you.

Qualifications

• Degree-qualified in Mechanical, Biomedical, or related engineering field.
• Experience in manufacturing, developing, or testing medical devices.

Responsibilities

• Drive product development projects from concept to launch.
• Collaborate with cross-functional teams for successful product delivery.

Skills

Problem-solving

Technical communication

Project documentation

Education

Degree in Mechanical Engineering

Degree in Biomedical Engineering

Tools

SolidWorks

Job description

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Product Development Engineer, bury st edmunds

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Client:

Six Ventures Ltd

Location:

bury st edmunds, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

4

Posted:

28.04.2025

Expiry Date:

12.06.2025

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Job Description:

Product Development Engineer – Medical Devices

We are proud to be partnering with an innovative and growing Medical Device company at the forefront of healthcare technology. We are supporting them in their search for a highly skilled and motivated Product Development Engineer to join their talented engineering team.

This is a fantastic opportunity for someone passionate about medical innovation and eager to make a real impact on patients’ lives through the development of advanced medical technologies.

Key Responsibilities:

• Drive product development projects from concept through to launch, adhering to ISO 13485 and FDA design control requirements.
• Collaborate with cross-functional teams including Quality, Regulatory, Clinical, and Manufacturing to ensure successful product delivery.
• Develop prototypes, perform testing, analyze data, and iterate designs based on technical and clinical feedback.
• Generate and maintain design documentation such as design history files (DHF), risk assessments, and technical reports.
• Support process validation and work closely with suppliers and manufacturing partners on DFM and scalability

Candidate Requirements:

• Degree-qualified in Mechanical, Biomedical, or a related engineering field.
• Previous practical experience in manufacturing, developing or testing of medical devices.
• Proficient in CAD (e.g., SolidWorks) and hands-on prototyping/testing.
• In-depth knowledge of design control processes and regulatory requirements.
• Excellent problem-solving, technical communication, and project documentation skills.

If you are ready to take the next step in your career and contribute to life-changing medical technology, we would love to hear from you.