.Descripción y detalle de las actividadesRoles & Responsibilities: - Manufacturing responsibility for tooling/fixtures, manufacturing equipment, and design improvements in production. - Provide mechanical design engineers with Design for Manufacturability (DFM) input to ensure consistency/commonality among hardware and standard part selections across product/sub-assembly lines. - Design, document, and create efficient "High-volume' manufacturing assembly line including: o Workplace and flow process development o Specify, document, procure, repair, maintain, qualify, and implement fixtures, hand tools, and equipment. o Determine and incorporate critical feature inspection and test checkpoints into the process. Document if discrepancies, actions, or steps are required. - Evaluate and help in the selection of suppliers for mechanical parts if required. Help resolve supplier quality issues. - Update and revise Manufacturing Process Instructions (MPIs) to ensure accuracy and completeness - Address line support issues as they arise - Document and report any variances, problems, issues, or concerns on all aspects of the manufacturing process - Review and disposition discrepant material. Implement corrective actions to prevent recurrences. - Active participant in quality improvement initiatives, providing feedback to find and solve the root cause of problems. - Evaluate designs for manufacturability (concerning tooling and assembly methods). Provide suggested change proposals, or tooling concepts during the early design process phase. - Design and documentation responsibilities for custom and standard production tooling/fixtures. - Process and part design/documentation duties for cost reductExperiência y requisitos- Demonstrate Mechanical and/or Process Engineering ability. - Demonstrate ability in failure analysis and continuous improvement. - BS degree in Mechanical Engineering or equivalent. - Minimum 2 years of mechanical or manufacturing engineering experience with Mid/high volume complex mechanism manufacturing. - Able to read and understand mechanical and electrical drawings. - Basic to Intermediate modeling experience (ProE, SolidWorks, or equivalent). - Possess strong communication skills to interact with suppliers, and other departments within the company (product development, planning, purchasing, regulatory, quality, etc.) - Prior experience working in an FDA/ISO-regulated environment (desirable). - Experienced in ISO 13485 or medical device manufacturing environment (desirable). - Prior experience with automated equipment, complex mechanism manufacturing, or robotics is a plus. - Experience with ASME Y14.5 Geometric Dimensioning and Tolerance. - Experience in Just-In-Time, Demand Flow Technology, and Lean Manufacturing techniques. - High English level (+ 70 %). - BSME required. - CAD experience preferred (ProE, AutoCAD). - Must be able to travel to the USAOrganizaciónIntuitive Surgical, S. de R.L de C.V