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Product Development Engineer
Product Development Engineer
Product Development Engineer
Posted 4 days ago
- Bedford, Bedfordshire
- Any
- External
Job Description Cure Talent are excited to partner with an innovative global medical organisation renowned for driving engineering excellence. We’re seeking a Product Development Engineer to join their team.
The new Product Development Engineer will be responsible for delivering robust solutions throughout the full product lifecycle. From concept generation through to design transfer and compliance, you’ll take ownership of the mechanical design output, ensure technical assurance, and actively contribute to innovation, quality, and delivery of breakthrough engineering solutions.
Key responsibilities:
Generate, evaluate and develop mechanical concepts in line with end-user requirements and manufacturing technologies
Lead or support engineering activities including prototyping, testing and risk analysis (FMEA)
Produce and maintain accurate technical documentation such as BOMs, drawings, specifications and design validation records
Collaborate cross-functionally to ensure designs meet regulatory requirements (ISO 13485, IVDR, FDA 21 CFR 820)
Communicate findings through written reports and presentations, contributing to project plans and stage-gate reviews
To be successful in this role, you will have:
A BEng in Mechanical Engineering (or equivalent) with proven industry experience, ideally within medical ...
The new Product Development Engineer will be responsible for delivering robust solutions throughout the full product lifecycle. From concept generation through to design transfer and compliance, you’ll take ownership of the mechanical design output, ensure technical assurance, and actively contribute to innovation, quality, and delivery of breakthrough engineering solutions.
Key responsibilities:
Generate, evaluate and develop mechanical concepts in line with end-user requirements and manufacturing technologies
Lead or support engineering activities including prototyping, testing and risk analysis (FMEA)
Produce and maintain accurate technical documentation such as BOMs, drawings, specifications and design validation records
Collaborate cross-functionally to ensure designs meet regulatory requirements (ISO 13485, IVDR, FDA 21 CFR 820)
Communicate findings through written reports and presentations, contributing to project plans and stage-gate reviews
To be successful in this role, you will have:
A BEng in Mechanical Engineering (or equivalent) with proven industry experience, ideally within medical ...