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An expanding medical device company based in Mildenhall, Suffolk is on the lookout for a hands-on Development Engineer to support the journey of new products from initial concept through to full-scale manufacture. This key role involves close collaboration with both design and production teams to ensure all products align with customer expectations, quality standards, and regulatory requirements at every stage of development.
What's the pay & hours?
- circa 32,000 - 36,000, based on experience
- Monday to Friday, full-time
- Long-term role with real growth and development opportunities
Key Responsibilities:
- Generate product documentation aligned with ISO 13485 and regulatory standards
- Develop and validate product test methods and evaluate design performance
- Collaborate with customers to gather and implement manufacturing requirements
- Support production line validation and process implementation
- Manage project timelines, budgets, and regular update reporting
- Work cross-functionally with engineering, supply chain, and vendors
- Contribute to internal and customer meetings, supporting project milestones
Who are we looking for?
- Practical experience with medical devices or regulated manufacturing
- Strong background in mechanical or medical-based engineering
- Skilled in documentation, data analysis, and MS Office tools
- Knowledge of regulatory frameworks (UKCA, MDR, FDA)
- Organised, independent, and confident communicator
Benefits:
- Be part of a company improving lives through medical innovation
- Supportive team environment with tailored training provided
- Opportunity to contribute to projects with real-world impact
- Occasional UK travel for project needs
If you're passionate about medical device development and ready to take on a new challenge, apply now or contact Brendan @ Prime Appointments to learn more.
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