MFG & PROCESS DVL ENGINEER II At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world. **Job Overview** Provides guidance and leadership on manufacturing processes in order to support organizational manufacturing goals; performs research on products and manufacturing process and share the same with senior engineers. **Job Requirements** + Developing production improvement goals; recommending suggestions for improvements to management. + Evaluating unfinished products and components; recommends quality and production improvements. + Analyzing statistics related to production efficiency, safety measures, and resource usage; research on effective ways of research with regards to cost saving. + Designing and evaluates plans for implementing manufacturing equipment, technology and resources to meet goals. **What your background should look like** **Key Responsibilities:** + New Product/Process Development + Execute process and test method validation along with design, develop, and qualify tooling/equipment + Using problem solving and DMAIC tools to solve processes and process improvements + New Product Introductions + Manage product transfers from new product development to operations or product transfers from site to site. + Develop bills of materials and assembly methods documentation while providing any training needed to technicians and assemblers. + Team Leadership (Primary) + An effective communicator that prepares status reports, modifies schedules, and manages project plans. + Communicate to stakeholders, customers, and others informed of project status and/or related issues + Ability to coordinate a team of engineers and technicians and direct technical work + Coach/mentor technical topics to junior engineers and technicians during product transfers + Collaborate effectively with other departments, including Quality, R&D, NPD, and Operations. + Project Management (Supporting) + Manage your project timelines and resources effectively. + Work with cross functional teams while being self-driven + Manage activities with risk to the project timelines, developing contingency plans, while outlining deliverables and milestones + Quality, Safety and Regulatory Compliance (Supporting) + Work with Quality Team to ensure all manufacturing processes and equipment comply with FDA regulations, ISO standards, and other relevant industry guidelines + Comply with safety and security procedures and report potentially unsafe conditions when using equipment and materials properly + Manage design requirements like Bioburden or Particulates, Biocompatibility and Cleanroom Environment compatibility **Required Skills & Experience** + Bachelor's degree in Engineering, Plastics, Chemical, Biomedical or Mechanical Engineering preferred + 4+ years of working experience in the Medical Device Industry + 2+ years of working experience in new production development or product transfers + Thorough understanding of Quality Management Systems (QMS) requirements that involve: + Process Mapping + Manufacturing Process Instructions + DOE and Process Characterization + OQ/PQ Protocol and Reports + IQ/OQ Protocols and Reports + PFMEAs + MVP/MVRs. + Experience in technically leading a team of engineers and technicians across multiple projects + Medical Device New Product Development which includes process development and characterization along with equipment/fixture design and qualification and test method and process validations + Preferred Skills & Experience + Hands-on experience with complex steerable or multi-lumen catheter assembly development and manufacturing with that includes manufacturing technologies with mandrel design, PTFE assembly, reflow, braiding, + tipping and extrusion + Experience with design controls, FDA regulation, GMP practices, and QSR requirements + CAD proficiency - SolidWorks and Mastercam + MS Office proficiency + Ability to achieve goals with effective planning and prioritization skills to meet immediate and long-range needs with independence + Must be well-organized, detail-oriented, with excellent oral and written communication skill + Green Belt (desirable) + American Visa (desirable) **Competencies** Values: Integrity, Accountability, Inclusion, Innovation, Teamwork Location: San Rafael, A, CR, 20108 City: San Rafael State: A Country/Region: CR Travel: 10% to 25% Requisition ID: 138520 Alternative Locations: Function: Engineering & Technology TE Connectivity and its subsidiaries, affiliates, and operating units (collectively, the "Company") is committed to providing a work environment that prohibits discrimination on the basis of age, color, disability, ethnicity, marital status, national origin, race, religion, gender, gender identity, sexual orientation, protected veteran status, disability or any other characteristics protected by applicable law or regulation.