Job Overview

Manufacturing Engineer I is responsible for optimizing, implementing, and standardizing manufacturing processes in manual, semi-automatic, and automatic environments. Analyzes production processes to improve efficiency, quality, and safety. Designs and adjusts tools and equipment, prepares technical documentation, and trains teams. Assists senior engineers in applying manufacturing techniques and machinery to enhance quality and output. Supports continuous improvement and the transfer of processes from development to mass production. Ensures key performance indicators such as First Pass Yield, scrap rates, CAPA closure, and cost reduction targets are met to maintain operational excellence.

Job Requirements

• Participate as a team member in projects and production support or improvement activities.
• Plan training and development objectives in coordination with the supervisor.
• Complete process design and development projects by training and guiding interns/technicians. 
• Identify and implement effective, permanent technical/system solutions to problems. 
•  Consistently meet customer requirements and demonstrate a commitment to performance excellence and on-time delivery.
•  Prepare product and process reports by collecting, analyzing, and summarizing information and trends 
• Ensure compliance with TE Connectivity systems and processes. 
• Identify and develop improvements to enhance key process metrics related to Service, Delivery, Quality, and Cost using Lean/6 Sigma methodologies. 
•  Research cutting-edge process technologies and evaluate their potential competitive advantage and cost benefits.
• Execute projects in coordination with other resources management functions (e.g.,NPI, Quality Engineering, Design Assurance, R&D, and other cross-functional departments) related to engineering. Work with the team to plan, coordinate, and implement activities that support the successful launch of new products, including make vs. Buy analysis, new process introduction, and more. Develop/modify manufacturing processes by studying product requirements and researching, designing, modifying, and testing manufacturing methods and equipment. • Maintain professional and technical knowledge by attending educational workshops and establishing personal networks. 
•  Manage external relationships with key technology vendors.
• Handle a variable workload to meet operational requirements. 
• Ensure compliance with all health, safety, and environmental regulations. 
• Coordinate and execute validation activities, including equipment IQ/OQ, process OQ/PQ, process characterization, attribute/variable test method validation, and associated documentation. 
•  Possess knowledge of how the Validation Master Plan connects to pFMEA, dFMEA, CAPA, NCE, Problem Solving, DMAIC, and risk management.
• Define, establish, and lead all required documentation to manage manufacturing processes, including analytical models, procedures, work instructions, employee training tools, process FMEAs, and more. 
• Knowledgeable in designing fixtures and tools for production. 
•  Execute TEBIT initiatives to generate cost-saving and continuous improvement projects. 

What your background should look like

• Strong communication, planning, and organizational skills. 
• Self-motivated and able to work independently. 
• Ability to make and implement decisions effectively. 
• Knowledge of medical devices or similar quality and manufacturing systems (Desirable)
•  Bachelor's degree in an Engineering field or equivalent, with 0-1 years of experience in a demanding high-volume production environment, or low-volume, high-mix manufacturing.
•  Statistical knowledge, including data analysis and the use of statistical software (JMP, Minitab, etc.)
•  Must be fluent in English, both written and spoken
•  Proficient user of CAD tools; SolidWorks experience preferred. Familiarity with Minitab, MS Project, and advanced Excel.
•  Understanding of engineering principles related to Six Sigma and/or Lean Manufacturing.

Competencies