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A medical device company is seeking a Senior Product Development Engineer to design and develop precision medical devices used in minimally invasive procedures. These products include highly engineered components requiring extremely tight tolerances and advanced manufacturing and assembly processes.
As part of the R&D organization, this role will work closely with manufacturing engineering, quality, and production teams to support both new product development and improvements to existing products. Responsibilities include leading development activities from concept through commercialization, as well as supporting sustaining engineering initiatives.
The ideal candidate brings strong mechanical engineering fundamentals, experience working within regulated medical device environments, and a structured approach to problem solving.
Design and develop precision mechanical components and systems for medical devices
Conduct engineering analyses, feasibility studies, and concept evaluations for new products and features
Define product requirements and perform design trade-off analyses to determine optimal solutions
Investigate product or process issues using structured root cause analysis methods
Maintain thorough technical documentation in accordance with medical device regulatory requirements
Collaborate with manufacturing teams on supplier selection, manufacturability, and design transfer
Support evaluation and implementation of engineering change orders
Research and evaluate new technologies, materials, and manufacturing techniques
Manage development activities including project plans, timelines, and resource coordination
Generate technical drawings for components, assemblies, and system interfaces
Provide sustaining engineering support for released products
Participate in a stage-gate product development process following medical device design control principles
Work closely with cross-functional teams including quality, regulatory, and operations
Contribute to innovative design concepts and proprietary manufacturing processes
Support competitive product and technology assessments
Proficiency in SolidWorks or similar 3D CAD software
Experience with finite element analysis (FEA) and GD&T
Demonstrated ability to apply structured engineering problem-solving methods
Experience working within regulated medical device environments
Familiarity with quality systems and design control requirements
Understanding of manufacturing and assembly processes for precision medical devices
Experience with sterilization methods and biocompatibility considerations
Experience supporting process validation activities (IQ/OQ/PQ)
Knowledge of risk management processes in product development
Experience with requirements definition, traceability, and verification/validation
Strong communication and collaboration skills across multidisciplinary teams
BS in Mechanical Engineering, Physics, or related discipline
8+ years of engineering experience
Advanced degree preferred
Experience performing root cause analysis methodologies such as DMAIC
Strong understanding of mechanics of materials
Familiarity with fluid or mechanical systems used in medical devices
Experience working with precision manufacturing or micro-scale components
Experience collaborating with external suppliers and manufacturing partners
Ability to fabricate simple tools or fixtures using standard machine shop equipment is a plus