Lead Mechanical Design Engineer

We are seeking a Lead Mechanical Design Engineer to drive the design, development and verification of complex medical devices across both capital equipment and disposable components. This hands‑on technical leadership role guides cross‑functional teams, oversees full lifecycle engineering, and delivers innovative, manufacturable and compliant solutions within a regulated environment.

• Lead the end‑to‑end design, development and verification of complex assemblies, sub‑assemblies, components and packaging.
• Select materials, manufacturing processes, tooling and automation solutions to meet performance, cost and scalability needs.
• Translate product requirements into detailed engineering specifications and conduct feasibility studies and proof‑of‑concept testing.
• Drive design and process optimisation to improve quality, performance and manufacturability.
• Lead risk‑management activities including PHA, FTA and dFMEA/uFMEA.
• Perform root‑cause analysis and implement corrective actions following failure investigations.
• Collaborate with manufacturing teams to troubleshoot issues and refine process parameters.
• Manage projects or sub‑projects, guide cross‑functional teams and apply structured project‑management methodologies.
• Support supplier and subcontractor activities and lead technical reviews with internal and external stakeholders.
• Provide team leadership including recruitment, performance oversight and daily activity coordination.
• Stay current with emerging engineering tools, technologies and methods to elevate team capability.

• 5+ years’ experience in medical device mechanical design, ideally spanning capital equipment and disposable components.
• Full product lifecycle experience: design, development, verification and optimisation.
• Strong background in material selection, manufacturing processes, GD&T, DFM/DFA, DOE and root‑cause analysis.
• Proven experience running risk‑management activities (PHA, FTA, dFMEA/uFMEA).
• Demonstrated project and team leadership, with clear ownership of deliverables and cross‑functional coordination.
• Bachelor’s or Master’s degree in Mechanical Engineering, Biomedical Engineering or equivalent.
• Deep understanding of design for manufacturability/assembly and modern engineering practices.
• Strong communication skills and ability to influence decisions through technical insight.
• Familiarity with medical device regulatory frameworks (ISO 13485, MDR, FDA 21 CFR 820).

We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate.

We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally.