PRODUCT ENGINEER II

Job Overview

TE Connectivity’s Product Engineering Teams optimize existing products from information or input provided by marketing, customers, Operation Teams, Development Engineers or other employees. They maintain existing products, processes, and specifications including modifications for new applications consistent with manufacturing techniques and economies. They also initiate and implement programs to continuously improve quality, and cost, while meeting customer requirements and may support and implement product extensions to existing platform products to meet specific customer requirements. They are the key experts in the products they are responsible for at TE.

What your background should look like:

To support the New Product development of Medical Devices 

RESPONSIBILITIES 

•    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 GDT 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

• Experience on FMEA documentation (PFMEA, DFMEA and Risk assessment)
• Will be responsible for establishing product requirements, concept prototyping, design and development (including verification and validation), risk/failure mode assessment, performance and safety testing
• Six Sigma Green Belt Holder
• Experience in working on Validation documentation (MVP, MVR, TMV. OQ, PQ protocols and Reports)
• Hands on experience on Statistical Analysis, Tool: Minitab
• Maintains detailed documentation throughout all phases of research and development.
• Reviews or coordinates outside vendor activities to support development.
• Interface with customers and internal departments articulating team activities and progress.
• Work closely with manufacturing engineering to improve process, procedure, and cost.

 

 

EDUCATION/KNOWLEDGE

•    Bachelor’s in engineering (Mechanical), M.S. in Engineering a plus. 
•    Demonstrated New product development experience 

Critical Experience

•    Minimum five or more years of related Medical product design and development engineering experience. 
•    Proven experience in product sustenance and product development-related documentation processes.
•    Well versed with product lifecycle management process.
•    Hands-on experience in SAP, Creo, SolidWorks, and Engineering Change management activities.
•    Hands-on experience using Minitab for capability study, gage R&R studies, Tolerance Stack-up Analysis and Process Improvement methodologies.

Competencies