Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Manage design assurance activities and ensure compliance with quality standards in medical device development.
- Company: Join a leading medical device manufacturer known for innovation and excellence in healthcare solutions.
- Benefits: Enjoy competitive pay, flexible working options, and opportunities for professional growth.
- Why this job: Make a real impact on healthcare by contributing to the development of life-saving medical devices.
- Qualifications: Degree in engineering or related field; experience in medical device design assurance is essential.
- Other info: Collaborate with cross-functional teams and gain hands-on experience in a dynamic environment.
The predicted salary is between 36000 - 60000 £ per year.
Cure Talent is delighted to be working with an innovative and well-established medical device manufacturer who is seeking a Design Assurance Engineer to support its growing product development team. This is an exciting opportunity to contribute to the development and introduction of new medical devices, ensuring compliance with regulatory and quality standards.
As their new Design Assurance Engineer, you will be responsible for managing design assurance activities, compiling technical documentation, conducting test analysis, and ensuring design control compliance. This role will involve working closely with quality, regulatory, and engineering teams to support successful product development and transfer into manufacturing.
- Oversee design assurance activities to ensure compliance with regulatory and quality standards
- Manage design control documentation, technical files, and risk management processes
- Support design verification and validation activities, including test planning and analysis
- Work closely with regulatory and quality teams to ensure successful product registration and compliance with ISO 13485 and other relevant standards
- Assist in process validation and manufacturing transfer to ensure product quality and performance
Qualifications:
- A degree in engineering, science, or a related technical field
- Experience in medical device design assurance, quality engineering, or regulatory compliance
- Strong knowledge of design control processes and documentation requirements
- Familiarity with ISO 13485 and other relevant medical device regulations
- Experience in risk management, verification and validation, and technical documentation
- Strong analytical skills with the ability to interpret complex data and ensure compliance
Locations
Design Engineer (Medical Devices) employer: Cure Talent
Contact Detail:
Cure Talent Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Design Engineer (Medical Devices)
✨Tip Number 1
Network with professionals in the medical device industry. Attend relevant conferences, webinars, or local meetups to connect with people who work in design assurance or related fields. This can help you gain insights into the role and potentially lead to referrals.
✨Tip Number 2
Familiarise yourself with ISO 13485 and other relevant regulations. Understanding these standards is crucial for a Design Assurance Engineer. Consider taking online courses or certifications that focus on regulatory compliance in medical devices to enhance your knowledge.
✨Tip Number 3
Prepare to discuss specific examples of your experience with design control processes and risk management during interviews. Be ready to explain how you've ensured compliance in past projects, as this will demonstrate your capability to handle the responsibilities of the role.
✨Tip Number 4
Stay updated on the latest trends and technologies in medical device design. Follow industry news, join relevant forums, and read up on recent innovations. This knowledge can give you an edge in discussions and show your passion for the field.
We think you need these skills to ace Design Engineer (Medical Devices)
Some tips for your application 🫡
Understand the Role: Read the job description thoroughly to grasp the key responsibilities and requirements for the Design Assurance Engineer position. This will help tailor your application to highlight relevant skills and experiences.
Highlight Relevant Experience: In your CV and cover letter, emphasise any previous experience in medical device design assurance, quality engineering, or regulatory compliance. Use specific examples to demonstrate your knowledge of ISO 13485 and design control processes.
Showcase Technical Skills: Make sure to include any technical skills that are relevant to the role, such as risk management, verification and validation, and your ability to compile technical documentation. This will show that you have the necessary expertise for the position.
Craft a Compelling Cover Letter: Write a personalised cover letter that connects your background to the company's mission and the specific role. Mention your enthusiasm for contributing to innovative medical devices and how your skills align with their needs.
How to prepare for a job interview at Cure Talent
✨Showcase Your Technical Knowledge
Make sure to brush up on your understanding of design control processes and ISO 13485. Be prepared to discuss how your previous experience aligns with the technical requirements of the role, especially in managing design assurance activities.
✨Demonstrate Your Analytical Skills
Since the role requires strong analytical skills, be ready to provide examples of how you've interpreted complex data in past projects. Discuss specific instances where your analysis led to improved compliance or product quality.
✨Prepare for Regulatory Questions
Expect questions related to regulatory compliance and quality standards. Familiarise yourself with the latest medical device regulations and be prepared to explain how you have ensured compliance in your previous roles.
✨Highlight Team Collaboration Experience
This position involves working closely with various teams. Share examples of how you've successfully collaborated with quality, regulatory, and engineering teams in the past to support product development and ensure compliance.
