Lead Mechanical Design Engineer, Limerick

Lead Mechanical Design Engineer

Job Description: The Lead Mechanical Design Engineer plays a pivotal role in the design, development, and verification of complex medical devices, encompassing both capital equipment and disposable components. The role demands a multidisciplinary engineering approach, integrating mechanical, mechatronic, electronic, and manufacturing expertise.Responsibilities

Lead and manage the design, development, and verification of complex assemblies, sub‑assemblies, components, and packaging. Select appropriate materials, processes, tooling, automation, and equipment to meet design and manufacturing needs. Translate product requirements into comprehensive product specifications.Conduct engineering studies and proof‑of‑concept testing to evaluate design feasibility. Drive design and process improvements to enhance performance, quality, and cost‑efficiency. Lead risk assessments including PHA, FTA, dFMEA/uFMEA for product and manufacturing processes. Perform root cause analysis and implement correctiveactions based on failure investigations.Collaborate with manufacturing teams to troubleshoot issues and optimize process parameters. Manage projects or sub‑projects, assigning tasks and guiding cross‑functional teams. Apply structured project management methodologies and communicate effectively with internal and external stakeholders.Research and integrate emerging technologies and development tools. Oversee recruitment, performance management, and development of direct reports. Coordinate and prioritize daily team activities to ensure timely task completion. Provide technical support to suppliers and subcontract manufacturers.Lead technical reviews and presentations across internal teams and external partners. Qualifications

Bachelor’s or Master’s degree in Mechanical or Biomedical Engineering (or equivalent). 6–9 years of experience in medical device design engineering, including at least 5 years leading mechanical design teams. Proven experience in developing both capital equipment and disposable medical device components.Strong foundation in engineering principles, root cause analysis, and documentation control. Proficient in GD&T and its application in design and inspection. Skilled in Design for Six Sigma (DFSS), statistical analysis, and DOE methodologies. Deep understanding of materials, manufacturing techniques, and design for manufacturability/assembly. Demonstrated leadership with clear ownership of deliverables and team outcomes.Strong analytical reasoning and ability to influence decisions through technical insight. Excellent communication skills and experience managing cross‑functional teams. Familiarity with medical device quality and regulatory systems (EN ISO13485, MDR, FDA CFR 820). Knowledge of Stage‑Gate or Product Development Life Cycle processes.EEO Statement

Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.

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