Overview
As a Mechanical Engineer, you will help develop new Medical Devices to ISO 13485 standards in a collaborative, state-of-the-art lab setting. You will join a multidisciplinary team of engineers and scientists to push the design and maturation of advanced electro-mechanical devices. The role focuses on turning complex technologies, such as handheld systems and microfluidics, into compliant products with meaningful clinical impact. This is a growth-driven opportunity at a Cambridge site with strong support for professional development.
Pay / Benefits
- salary
- pension
- bonuses
- healthcare
- other benefits typical of larger organisations
Responsibilities
- Develop new Medical Devices in compliance with ISO 13485
- Collaborate with Mechanical, CAD, Electronics engineers, physicists and scientists on device development
- Design and qualify complex handheld and microfluidic technologies
- Work within a regulated environment to advance product milestones
- Leverage state-of-the-art laboratories and workshops to accelerate development
- Support cross-functional activities across regulatory, quality, and design reviews
Key requirements
- Mechanical Engineering degree from a leading university
- 2–10 years of relevant experience in Medical Devices; senior candidates considered
- Experience in successfully developing brand-new Medical Devices to ISO 13485
- Background in regulated environments; life sciences or aerospace backgrounds considered
- Knowledge of mechanical design best practices in complex electro-mechanical systems
- Collaborative team player
- Effective communication across multidisciplinary teams
- Problem-solving and proactive approach
- Mechanical design for Medical Devices
- ISO 13485 experience
- Handheld device development
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