.What Manufacturing Engineering contributes to Cardinal HealthEngineering is responsible for performing research and analyses to develop design options for components, products, systems and processes.Manufacturing Engineering is responsible for developing manufacturing processes, production floor layouts and associated tools. Reviews new designs for manufacturability. Designs process improvements to reduce product cost, process cycle time and improved product quality.Job SummaryThe Senior Engineer, Manufacturing oversees and project manages large engineering projects. This job serves as the technical lead for both internal and external engineering teams. The senior engineer is responsible for the management of projects from start to end from both a resource management and outcome perspective. This job leads teams as necessary but is not a people manager.ResponsibilitiesManages the coordination and overall integration of technical activities in engineering projects.Designs mechanical changes to manufacturing machines.Selects parts and materials for applicable design changes.Directs, reviews, or approves project design changes.Documents design changes.Evaluates mechanical processes and identifies areas for improvement.Implementing design changes in the applicable facilities/production lines.Design and implement the processes that comply with the product requirements and high operational performance.Document all processes according to the ISO Quality system and FDA.Respond opportunely to the LAPS, identifying the root cause of the deviations to the system.Identify and minimize the sources of Scrap.Plan and execute OPEX projects.Design technical and operational training.Keep the PFMEA updated.Execute the process validations according to the MVP.Define capacity increase needs.Support new product projects.Solution of productivity and scrap quality problems by applying analysis and optimization techniques.Keep the cost of products updated.Comply with the necessary security measures to prevent accidents, occupational diseases and environmental contingencies within the company.Comply with the environmental measures established in the Internal Work Regulation.Coordinate and implement the QIP / COS initiative in the process area.CAPEX project management (Capital and Expenses).Generate engineering documentation to support validations and engineering changes.Qualifications2-4 years of experience, preferred.Bachelor's degree in related field, or equivalent work experience, preferred.Advanced English.Knowledge: New Product Introduction, Product Transfer, Agile, BPCS, Product Costing, Patient Focused, MS Project, Process and Product validations, Project Management, Six Sigma, Lean Manufacturing, ISO13485 / ISO9001, FDA or equivalent.What is expected of you and others at this levelApplies working knowledge in the application of concepts, principles and technical capabilities to perform varied tasks.Works on projects of moderate scope and complexity