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About Cambridge Mechatronics Ltd

Cambridge Mechatronics Ltd (CML) is a globally recognised fabless semiconductor company headquartered in Cambridge, UK. CML is pioneering Shape Memory Alloy (SMA) actuator systems that deliver breakthrough performance in high-precision, high-volume applications such as smartphones, AR/VR head-mounted devices, and compact medical devices.

With a multi-disciplinary global team spanning materials science, mechanical design, electronics, and software, CML develops complete actuator system solutions — including SMA actuators, control ICs, and advanced algorithms.

CML holds approximately 900 granted and pending patents and ranks among the top 25 UK patent filers, reflecting our strong commitment to innovation and technology leadership.

We are now seeking a motivated and hands-on Development & Verification Engineer to support the development of our next-generation miniature insulin pump.

The Role

Working alongside the Head of Medical, the Development & Verification Engineer will support the build, integration, testing, and performance evaluation of a novel insulin pump system.

This is a practical, multidisciplinary engineering role suited to a self-starter who is adaptable, organised, and comfortable working in a fast-paced development environment. The successful candidate will play a key role, taking ownership of the process from managing prototype builds, maintaining test activities, troubleshooting technical issues, and improving engineering processes while working within a regulated medical device environment compliant with ISO13485.

Key Responsibilities

· Manage the build and assembly activities for insulin pump development systems and prototypes, including coordination, issue tracking, and build documentation

o Debug build and integration issues across mechanical, electrical, and systems interfaces

o Support and improve engineering build processes and workflows

· Plan and deliver performance verification and life testing activities

o Write test specifications, protocols, and technical reports

o Set up and maintain test rigs and equipment, including environmental and test chamber activities

o Provide first-line debugging and troubleshooting support when test systems or rigs fail

o Conduct data analysis and present test findings clearly to the engineering team

· Support engineering investigations and research activities on subsystems and critical parameters

· Work collaboratively with firmware, electronics, mechanical, and systems engineering teams

· Contribute to continuous improvement initiatives and implementation of new engineering processes

· Ensure all development and testing activities are carried out in accordance with ISO13485 quality standards

Skills & Experience

Essential

· Degree in engineering, science, or a related discipline

· Hands-on engineering experience within a development or test environment

· Strong practical problem-solving and debugging skills

· Mechanical and systems engineering understanding

· Experience supporting engineering builds and test activities

· Ability to work independently and proactively

· Strong organisational and communication skills

· Adaptable mindset with willingness to support a wide range of engineering activities

· Experience working within quality-driven engineering processes

Desirable

· Experience within a medical devices or regulated industry environment

· Knowledge of ISO13485 and medical device development processes

· Experience with environmental or life testing

· Ability to modify or write basic test code/scripts

· CAD experience

· Experience setting up and maintaining engineering test rigs

· Experience with data analysis and technical reporting

Personal Attributes

· Self-motivated and hands-on

· Adaptable and flexible approach to engineering challenges

· Strong attention to detail and quality

· Collaborative team player

· Practical mindset with a willingness to take ownership

· Enthusiastic about developing innovative medical technologies

Why Join CML?

This is an exciting opportunity to join a world-class technology company applying its expertise to innovative medical devices that can improve patients’ lives globally. You will work in a collaborative, multidisciplinary environment and contribute directly to the development of next-generation insulin delivery technology.