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- Tasks: Lead product development from design to market, ensuring safety and usability.
- Company: Join an innovative MedTech company transforming patient care in surgical environments.
- Benefits: Enjoy a dynamic work environment with opportunities for professional growth and impact.
- Why this job: Be at the forefront of medical device innovation, making a real difference in patient outcomes.
- Qualifications: 5+ years in medical device R&D, strong ISO 13485 experience, and an engineering degree required.
- Other info: This role requires EU work permit; perfect for those passionate about healthcare technology.
The predicted salary is between 42000 - 84000 £ per year.
Cure Talent are delighted to be partnering with an innovative MedTech company dedicated to transforming patient safety, monitoring and outcomes in invasive vascular and surgical care. We’re seeking an experienced engineer with deep working knowledge of ISO 13485 and proven capability across the post-design, full product lifecycle. You’ll be the technical lead, taking products from design through to successful manufacture and market release, managing all critical phases: Usability, Risk, V&V, Documentation, and Transfer to Manufacture.
Key Responsibilities Include:
- Leading post-design development across usability, human factors, and risk analysis incl. FMEA
- Driving design verification and validation, planning and executing V&V strategies
- Managing smooth transfer to manufacture and serving as liaison with CMOs
- Defining and maintaining BoMs, materials, and supporting design for manufacture principles
What We’re Looking For:
- 5+ years in medical device R&D or development, with ownership of post-design activities and an engineering or scientific degree
- Strong experience working under ISO 13485, with full DHF and regulatory documentation responsibility
- Skilled in usability engineering, human factors, and risk management e.g. FMEA
- Solid understanding of V&V processes and manufacturing transfer
If you’re eager to be at the forefront of medical device development and work with a company that prioritizes patient outcomes, we’d love to hear from you!
Product Development Engineer employer: JR United Kingdom
Contact Detail:
JR United Kingdom 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 the specific requirements for medical device development. Understanding these standards will not only help you in interviews but also demonstrate your commitment to quality and compliance in the industry.
✨Tip Number 2
Network with professionals in the MedTech field, especially those who have experience in product development. Attend industry events or join relevant online forums to connect with potential colleagues and learn more about the latest trends and challenges in the sector.
✨Tip Number 3
Prepare to discuss your previous experiences in managing post-design activities, particularly in usability engineering and risk management. Be ready to share specific examples of how you've successfully led projects through the V&V process and ensured smooth transitions to manufacturing.
✨Tip Number 4
Research Cure Talent and the innovative MedTech company they are partnering with. Understanding their mission, values, and recent developments will allow you to tailor your conversations and show genuine interest during the application process.
We think you need these skills to ace Product Development Engineer
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in medical device R&D, particularly focusing on post-design activities. Emphasise your knowledge of ISO 13485 and any relevant projects you've led.
Craft a Compelling Cover Letter: In your cover letter, express your passion for improving patient safety and outcomes. Mention specific examples of how you've successfully managed product lifecycles and your familiarity with V&V processes.
Highlight Relevant Skills: Clearly outline your skills in usability engineering, risk management, and documentation. Use industry-specific terminology to demonstrate your expertise and understanding of the role.
Proofread Your Application: Before submitting, carefully proofread your application for any errors or inconsistencies. A polished application reflects your attention to detail, which is crucial in the medical device field.
How to prepare for a job interview at JR United Kingdom
✨Know Your ISO 13485 Inside Out
Since the role requires strong experience with ISO 13485, make sure you can discuss your knowledge and experience with this standard in detail. Be prepared to give examples of how you've applied it in past projects.
✨Demonstrate Your V&V Expertise
The interviewers will be keen to understand your approach to verification and validation. Prepare to explain your strategies for planning and executing V&V processes, and share specific instances where your efforts led to successful outcomes.
✨Showcase Your Leadership Skills
As a technical lead, you'll need to demonstrate your ability to manage teams and projects effectively. Think of examples where you've successfully led post-design development or collaborated with cross-functional teams to achieve project goals.
✨Prepare for Technical Questions
Expect technical questions related to usability engineering, risk management, and manufacturing transfer. Brush up on these topics and be ready to discuss how you've tackled challenges in these areas during your career.
