SummaryLead Mechanical Design Engineer responsible for the design, development, and verification of complex medical devices including capital equipment and disposable components. This role combines deep technical leadership with project and people management to deliver compliant, manufacturable, and high-performance solutions.ResponsibilitiesLead the design, development, and verification of complex assemblies, sub-assemblies, components, and packagingTranslate user and product requirements into detailed technical specifications and design outputsSelect materials, manufacturing processes, tooling, automation, and equipment aligned with performance and scalability needsConduct feasibility assessments, engineering analyses, and proof-of-concept testingDrive continuous improvement initiatives focused on quality, performance, robustness, and costLead product and process risk assessments including PHA, FTA, dFMEA, and uFMEAPerform root cause analysis and define corrective and preventive actionsPartner with manufacturing teams to resolve technical issues and optimise process capabilityManage projects and sub-projects using structured project management methodologiesProvide technical leadership to cross-functional teams and external suppliersLead technical design reviews, presentations, and decision-making forumsOversee recruitment, performance management, and development of direct reportsCoordinate and prioritise daily team activities to meet programme timelinesStay current with emerging technologies, tools, and engineering best practicesRequirementsBachelor's or Master's degree in Mechanical Engineering, Biomedical Engineering, or equivalent6–9 years' experience in medical device design engineering, including 5+ years in a leadership roleExperience designing both capital equipment and disposable medical devicesStrong grounding in mechanical engineering principles and failure investigation techniquesAdvanced application of GD&T for design and inspectionExperience with Design for Six Sigma, statistical analysis, and DOEStrong understanding of materials, manufacturing processes, and DFM/DFAProven technical leadership with ownership of deliverables and outcomesExcellent analytical, problem-solving, and communication skillsWorking knowledge of ISO 13485, MDR, FDA CFR 820, and regulated design controlsExperience with Stage-Gate or Product Development Lifecycle processesHigh attention to detail and strong documentation disciplineBenefitsComprehensive healthcare coverage, including options for family membersCompetitive pension scheme with employer contributionPerformance-related incentive bonusOpportunity to participate in a company share investment or savings programmeLife assurance coverGenerous annual leave entitlement plus public holidays