Senior Mechanical Engineer

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised. What You Can Expect As a Senior Mechanical Engineer, you will act as a senior technical individual contributor and technical lead for complex mechanical engineering activities related to existing products and manufacturing processes. This role requires deep engineering expertise, strong independent judgment, and the ability to lead technical work across cross-functional teams without formal people management responsibilities. You will be expected to identify technical risks, diagnose complex product and process issues, develop robust engineering solutions, and guide implementation in a regulated medical device environment. Success in this role requires a hands-on, analytical engineer who can move effectively between design, manufacturing, quality, supplier, and regulatory considerations. How You'll Create Impact Lead the technical execution of product improvement initiatives for existing products, from problem definition through engineering assessment, solution development, verification, implementation, and releaseServe as a technical contributor for cross-functional activities involving engineering, production, quality, suppliers, and new product development partnersOwn complex engineering analyses to support design changes, production issue resolution, and product performance improvement, including dimensional, tolerance stack-up, functional, structural, and failure mode assessmentsIndependently investigate product and process nonconformances, customer complaints, and technical issues by identifying root causes, assessing risk, and recommending practical, data-driven corrective actionsDefine, plan, and execute verification and validation activities associated with engineering changes using scientifically and statistically sound methodsDevelop test methods, protocols, and engineering rationales to support product modifications, design decisions, and manufacturing improvementsEvaluate the impact of design or process changes on product performance, manufacturability, reliability, quality, and regulatory complianceCoordinate implementation and transfer of product improvements to suppliers and manufacturing teams, ensuring technical requirements are clearly defined and effectively executedContribute technical expertise to risk management activities, including FMEA and related engineering risk assessments.Support CAPA, nonconformance, and complaint investigation activities with strong technical analysis and clear documentationProvide engineering documentation and technical support for regulatory submissions, product certifications, and change control activities, including support for 510(k)-related documentation where applicable What Makes You Stand Out Significant experience in the medical device industry or another highly regulated manufacturing environmentExperience working within an ISO 13485-regulated environmentStrong experience with engineering change implementation for released productsExperience with risk management activities, including DFMEA and structured engineering risk evaluationExperience planning and executing verification and validation (V&V) activitiesFamiliarity with 510(k) submission support activities and the documentation expectations associated with regulated product changesStrong capability in tolerance stack-up analysis for mechanical assembliesStrong knowledge of geometric dimensioning and tolerancing (GD&T)Hands-on experience with prototyping, inspection, manufacturing support, and supplier collaborationStrong root-cause investigation and corrective action skillsStrong technical writing and documentation skills in a regulated environment Your Background Bachelor’s degree in Mechanical Engineering or a related engineering disciplineMinimum of 5 years of relevant engineering experience, or an equivalent combination of education and experienceStrong in-depth mechanical engineering fundamentals, including design analysis, failure analysis, and manufacturabilityProficiency with 3D CAD tools; SolidWorks experience preferred Travel Expectations This is a senior technical individual contributor role and does not include direct people management responsibility. Travel up to 30% EOE/M/F/Vet/Disability