Product Engineer II

• Work with global multi-functional project teams to support on technical and SAP documentation
• Manage sustenance engineering tasks for medical products and related documentation
• Understand the functional requirements of a product and ensure that the design changes meet the functional requirement
• Work with SAP, PLM, EC applications and ENG. doc. management systems.
• Review and understand BOMs, routers and Inspection Plans/ROS according to requirements
• Work on trails data, carryout statistical analysis, and reports
• Generate 3D models (Plastic & Sheet metal) & drawings using Creo / SolidWorks using any PLM/PDM tools
• Creating technical documentations as per change requests and prompt response
• Deliver required documents as part of phase gate process
• Knowledge on Tolerance Stack-up Analysis, Validation documentation and GD&T will be added advantage
• Look for the opportunities of improvement and implement process improvement ideas.
• Properly document and internally communicate all technical discoveries, inventions, and intellectual property. Maintain confidential and proprietary information and communications as property of TE
• Continuous Improvement: Identify and work with key business stakeholders and operations teams to implement improvement opportunities using Lean and six-sigma tools.
• Service: Ensures that Exceptional Customer Experience (ECE) for both the Internal and External customers are met by meeting or exceeding commitments.
• Responsible for managing the overall equipment performance (OEE) through the appropriate use of Lean Manufacturing tools and techniques (TPM etc.)
• Ensure equipment preventative maintenance procedures are effective and ensure compliance to preventative maintenance program.
• Introduction of new equipment; equipment installation validation, process development and validation.
• Resolve quality and technical issues such that impact on product supply to customers is minimized and support Business Unit CAPAs, NCs, FMEAs and audit prep activities.
• Develop and manage SOPs / manufacturing standards / operations standard work as required in compliance with change control process.

• Bachelors in engineering (Mechanical), M.S. in Engineering a plus.
• Demonstrated product development experience
• Minimum 5 or more years of related Medical product design and development engineering experience.
• Proven experience in product sustenance and product development related documentation process.
• Well versed with product lifecycle management process.
• Hands on experience in SAP, Creo, SolidWorks, Engineering Change management activities.
• Hands on experience using Minitab for capability study, gage R&R studies, Tolerance Stack-up Analysis and Process Improvement methodologies.
• Demonstrate a practical understanding of Lean Manufacturing principles and statistics.

Competencies

• Innovative mechanical design skills.
• Can-do attitude, resourceful, action oriented, and drive for results.
• Good problem solving and project management skills.
• Ability to effectively manage and motivate others to meet deadlines.
• Networks with key contacts outside own area of expertise and experience working with overseas suppliers/customers. Willing to travel globally if needed.
• Demonstrated excellent written and oral communication skills in English language