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A growing medical device manufacturer in Mildenhall, Suffolk, is seeking an enthusiastic Development Engineer to support the transition of new products from concept to full-scale production. You'll play a vital role in bridging design and manufacturing, ensuring products meet regulatory and quality standards while aligning with customer needs.
What's the pay & hours?
- circa 32,000 - 34,000, 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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