Job Information
Hologic Product Development Engineer in Cambridge, United Kingdom
Product Development Engineer
Cambridge, Cambridgeshire, United Kingdom
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 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 our development programs with a focus on hands on mechanical design and development of components, instruments, sub-assemblies and disposable devices within our Breast Surgery product portfolio. You will define requirements, design and prototype solutions, and lead verification/validation activities within a regulated environment (ISO 13485). You will 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 mechanical design of product and sub-assemblies from concept through detailed design, prototyping and verification/validation, ensuring safety, performance and manufacturability
Perform mechanical architecture, materials selection, tolerance analysis (GD&T). Design for manufacture, assembly and serviceability; generate CAD models and drawings
Project manage work streams: build and track plans, risks and budgets, drive decisions, report status, ensure delivery to ISO 13485 design controls
Lead relationships with external partners (suppliers, consultants, contract manufacturers)
Ensure robust risk management (ISO 14971) and compliance with relevant standards
Collaborate closely with cross-functional teams including Product Engineering, Quality, Marketing, Regulatory Affairs, and our Implantables Team.
Prepare and maintain detailed documentation for all design and development activities including design specifications, test protocols and compliance reports.
KNOWLEDGE, SKILLS & EXPERIENCE
Educational background in Mechanical Design, Materials Engineering, (or a related field) or equivalent experience in mechanical product development within regulated industries
Knowledge of CAD (e.g. SolidWorks), GD&T, materials and plastics selection, tolerance stack-ups, DFM/DFA
Project management skills—able to plan, prioritise, and keep teams on track and experience leading external suppliers/contractors
Experience with design verification and validation, and working through product development phases
Working knowledge of ISO 13485, ISO 14971, ISO 10993, IEC 62366
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.
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