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Product Development EngineerHologic • Cambridge, England, United Kingdom
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Product Development Engineer

Hologic
  • GB
    Cambridge, England, United Kingdom
  • GB
    Cambridge, England, United Kingdom
Apply Now

About

Product Development Engineer

Role location: Cambridge, UK

Discover a career with real meaning. One that offers the opportunity to showcase your talents, achieve measurable success and gain immense satisfaction by shaping the future of cancer care. 

At Endomag, a Hologic company, we’re redefining cancer treatment and empowering clinicians worldwide with innovative medical solutions. 

We’re now looking for a talented Product Development Engineer to join our dynamic team in Cambridge —someone with a strong passion for Physics, Electronics and Software who thrives on solving complex challenges, driving excellence, and making an impact that truly matters.

As Product Development Engineer at Endomag, a Hologic company, you will play a critical role in the development of next‑generation medical devices. This is a highly hands‑on position focused on electro‑mechanical system design, experimental development and signal processing. You will define requirements, design and prototype solutions and lead verification/validation activities within a regulated environment (ISO 13485). You’ll collaborate closely with a network of third‑party suppliers, contract development organisations, consultants and internal cross‑functional teams to deliver innovative, compliant and manufacturable products.

KEY RESPONSIBILITIES

Own electromechanical design of products and sub-assemblies from concept through detailed design, prototyping, and verification/validation

Design, build and refine experimental rigs and test setups

Develop and optimise signal processing algorithms supporting device performance

Plan and execute verification and validation (V&V) activities, including data analysis and clear technical reporting

Collaborate closely with cross-functional teams including R&D, Product Engineering, Quality, Marketing, Regulatory Affairs to translate user needs into robust design solutions

Lead relationships with external partners (suppliers, consultants, development partners)

Ensure development activities comply with ISO 13485 and relevant medical device standards, including: ISO 14971 (Risk Management), IEC 62304 (Medical Device Software), IEC 60601 1 (Electrical Safety)

Prepare and maintain high quality design documentation, including requirements, specifications, test protocols, and reports

KNOWLEDGE, SKILLS & EXPERIENCE

Educational background in Physics, Physical Sciences, Electronics Engineering (or closely related field) or equivalent experience in product development within regulated industries

Experience with experimental development, testing and data analysis

Exposure to signal processing, modelling, or algorithm development

Experience using engineering and modelling tools such as MATLAB, LabVIEW, SPICE, COMSOL or similar

Comfortable working at the interface of hardware, software, and systems engineering

Excellent problem-solving and communication skills and a collaborative team spirit

Eager to learn, with a drive for continuous improvement

Ready to Make an Impact?

If you have the right skills and experience and want to join our team, apply today. We can’t wait to hear from you!

Innovate with Purpose: Work at the forefront of life-changing medical technology.

Collaborative Culture: Join a friendly, supportive team where your contributions matter.

Personal Growth: Expand your skills in a fast-growing, global company. 

#LI-KP1

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  • Cambridge, England, United Kingdom

Languages

  • English
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