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- Tasks: Join us to develop cutting-edge medical devices from concept to launch.
- Company: Be part of an innovative company leading the way in medical technology.
- Benefits: Enjoy a permanent role with opportunities for growth and learning.
- Why this job: Make a real impact in healthcare while working in a dynamic, collaborative environment.
- Qualifications: Degree in Engineering and two years' experience in medical device development required.
- Other info: Familiarity with key quality standards is a plus!
The predicted salary is between 36000 - 60000 £ per year.
Cure Talent are thrilled to be partnering with an innovative company who are at the forefront of developing Medical Devices. We are looking for a Product Development Engineer where you will play a crucial role in ensuring the full traceability of the product development process working from initial requirements to final validation.
Play a key role in the development of new medical devices, from concept to commercial launch, ensuring compliance with regulatory standards.
- Create and maintain technical documentation, including design history files, risk management files, and technical files.
- Collaborate with subcontract manufacturers to implement design for manufacture and assembly, supporting smooth design transfer.
- Provide technical expertise for regulatory submissions, QMS compliance audits, and remediation of legacy products.
Degree in Engineering (Electronics, Mechanical, or Manufacturing).
A minimum of two years of experience in medical device development or a similarly regulated industry, with a track record of delivering innovative products to market.
Familiarity with IEC 60601, ISO 13485, and ISO 14971 quality and risk management standards.
If you’re eager to be at the forefront of medical device development and work with a company that prioritises innovation, we’d love to hear from you!
Product Development Engineer (Permanent) employer: Cure Talent
Contact Detail:
Cure Talent Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Product Development Engineer (Permanent)
✨Tip Number 1
Familiarise yourself with the latest trends and technologies in medical device development. This will not only help you understand the industry better but also allow you to speak confidently about how your skills align with the company's innovative approach.
✨Tip Number 2
Network with professionals in the medical device field, especially those who have experience with IEC 60601, ISO 13485, and ISO 14971 standards. Engaging in conversations with them can provide valuable insights and potentially lead to referrals.
✨Tip Number 3
Prepare to discuss specific examples from your past work that demonstrate your ability to manage the product development process from concept to launch. Highlight any challenges you faced and how you overcame them, particularly in a regulated environment.
✨Tip Number 4
Showcase your collaborative skills by preparing to discuss how you've worked with cross-functional teams or subcontract manufacturers in the past. Emphasising your ability to facilitate smooth design transfers will resonate well with the hiring team.
We think you need these skills to ace Product Development Engineer (Permanent)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in medical device development or regulated industries. Emphasise your familiarity with standards like IEC 60601 and ISO 13485, as well as any specific projects that showcase your skills in product development.
Craft a Compelling Cover Letter: In your cover letter, express your enthusiasm for the role and the company. Discuss how your background aligns with their needs, particularly your experience in ensuring compliance with regulatory standards and your ability to manage technical documentation.
Showcase Technical Expertise: When detailing your experience, be specific about your contributions to product development processes. Mention any direct involvement with design history files, risk management files, and your role in regulatory submissions to demonstrate your technical expertise.
Highlight Collaborative Skills: Since the role involves collaboration with subcontract manufacturers, include examples of successful teamwork in your application. Describe how you’ve supported design transfers or worked with cross-functional teams to achieve project goals.
How to prepare for a job interview at Cure Talent
✨Understand Regulatory Standards
Make sure you have a solid grasp of IEC 60601, ISO 13485, and ISO 14971. Be prepared to discuss how your experience aligns with these standards and how you've applied them in previous roles.
✨Showcase Your Technical Documentation Skills
Be ready to talk about your experience creating and maintaining technical documentation. Highlight specific examples of design history files or risk management files you've worked on, as this is crucial for the role.
✨Demonstrate Collaboration Experience
Since the role involves working with subcontract manufacturers, share examples of how you've successfully collaborated with others in the past. Emphasise your ability to support smooth design transfers and implement design for manufacture.
✨Prepare for Problem-Solving Questions
Expect questions that assess your problem-solving skills, especially regarding regulatory submissions and QMS compliance audits. Think of scenarios where you've had to troubleshoot issues and be ready to explain your thought process.
