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- Tasks: Join us as a Development Engineer, bringing innovative medical devices from concept to production.
- Company: We're a growing medical device company in Mildenhall, dedicated to improving lives through innovation.
- Benefits: Enjoy a supportive team, tailored training, and opportunities for occasional UK travel.
- Why this job: Make a real-world impact while collaborating with passionate teams in a dynamic environment.
- Qualifications: Experience in medical devices or regulated manufacturing is essential; strong communication skills are a must.
- Other info: Competitive salary of £32,000 - £36,000, with long-term growth opportunities.
The predicted salary is between 28000 - 36000 £ per year.
An expanding medical device company based in Mildenhall, Suffolk, is looking for a proactive Development Engineer to play a key role in bringing new products from initial concept through to full-scale production. This hands-on position involves close collaboration with both the design and production teams to ensure each product meets customer expectations, quality benchmarks, and regulatory standards throughout 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.
Product Development Engineer employer: Prime Appointments
Contact Detail:
Prime Appointments Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Product Development Engineer
✨Tip Number 1
Familiarise yourself with ISO 13485 and other relevant regulatory standards. Understanding these frameworks will not only help you in interviews but also demonstrate your commitment to quality and compliance in product development.
✨Tip Number 2
Network with professionals in the medical device industry. Attend relevant conferences or workshops, and connect with people on platforms like LinkedIn. This can provide insights into the company culture and potentially lead to referrals.
✨Tip Number 3
Prepare to discuss specific projects where you've collaborated cross-functionally. Highlighting your experience in working with design and production teams will show that you can effectively contribute to the role's key responsibilities.
✨Tip Number 4
Research the company’s recent projects and innovations in medical devices. Being knowledgeable about their work will allow you to ask insightful questions during interviews and demonstrate your genuine interest in their mission.
We think you need these skills to ace Product Development Engineer
Some tips for your application 🫡
Understand the Role: Read the job description thoroughly to understand the key responsibilities and required skills for the Product Development Engineer position. Tailor your application to highlight your relevant experience in medical devices and regulated manufacturing.
Highlight Relevant Experience: In your CV and cover letter, emphasise your practical experience with medical devices, your background in mechanical or medical-based engineering, and any specific projects that demonstrate your skills in documentation and data analysis.
Showcase Your Skills: Make sure to mention your proficiency in MS Office tools and your knowledge of regulatory frameworks such as UKCA, MDR, and FDA. Provide examples of how you've used these skills in previous roles to meet quality benchmarks and regulatory standards.
Craft a Compelling Cover Letter: Write a cover letter that not only outlines your qualifications but also expresses your passion for medical device development. Mention why you want to work for this expanding company and how you can contribute to their mission of improving lives through medical innovation.
How to prepare for a job interview at Prime Appointments
✨Understand the Regulatory Standards
Familiarise yourself with ISO 13485, UKCA, MDR, and FDA regulations. Being able to discuss how these standards impact product development will show your knowledge and commitment to quality.
✨Showcase Your Collaboration Skills
Prepare examples of how you've successfully worked with cross-functional teams in the past. Highlighting your ability to communicate effectively with design and production teams will demonstrate that you're a team player.
✨Demonstrate Problem-Solving Abilities
Be ready to discuss specific challenges you've faced in previous roles and how you overcame them. This will illustrate your proactive approach and ability to manage project timelines and budgets.
✨Prepare for Technical Questions
Brush up on your technical knowledge related to medical devices and mechanical engineering. Expect questions about product test methods and design performance evaluation, so be prepared to discuss your experience in these areas.
