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 Appointments to learn more.