Job ID: [[id]]
Job Code: 30004621
Business Unit: MEDICAL (50126885)
Building: Sahasra Shree (N84)
Band/Level: 5
Hiring Manager: Nimbennappa Gani
Relocation: Yes – Domestic
Travel: 10% to 25%
Employee Referral Amount: ₹20,000.00
Education Experience: Bachelors Degree (High School +4 years)
Employment Experience: 5-7 years

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
TE Connectivity’s R&D/Product Development Engineering Teams conceive original ideas for new products, introduce them into practice. They are responsible for product development, and qualification from market definition through production and release; assist in the qualification of suppliers for new products to ensure suppliers deliver quality parts, materials, and services for new or improved manufacturing processes; conduct feasibility studies, testing on new and modified designs; direct and support detailed design, testing, prototype fabrication and manufacturing ramp. The R&D/Product Development Engineering Teams provide all required product documentation including, but not limited to, Solid Model, 2D/3D production drawings, product specifications, and testing requirements. They create and modify detailed drawings and drafting or conceptual models from layouts, rough sketches or notes and contribute to design modifications to facilitate manufacturing operation or quality of product. Typical fields of expertise include: materials, mechanics and systems, electrical, optics, chemistry, software, automation systems, packaging, testing and measurement, and manufacturing of electrical, mechanical and electronic components, products, and their integration into systems.

TE’s Medical business unit, part of the Industrial Solutions segment, offers medical device OEMs, a complete product offering, and capability portfolio for minimally invasive, imaging, surgical, diagnostic, and therapeutic device. With more than 350 design engineers and a global presence in all key medical device hubs, we are a premier partner to the world’s leading medical technology companies for their next-generation medical devices. We are experts in all aspects of device design and manufacture, from access & delivery solutions for interventional medicine, to sensors & connectors for surgical applications. Our innovative solutions enable groundbreaking medical therapies such as treating heart disease without opening the body, placing microscopic devices into brain arteries and powering robotic surgery.

The Research and Development Engineer is responsible for providing engineering knowledge, skill and ability to handle such tasks as: project management, engineering design, prototyping development, gathering of pertinent background information and leading project and design teams from conception through commercial launch of medical devices. Additionally, the Research and Development Engineer will be responsible for procuring material quotes, interacting with customers while ensuring full compliance to FDA QSR (21 CFR 820) and applicable ISO 13485 requirements.
Will be responsible for establishing product requirements, concept prototyping, design and development (including verification and validation), risk/failure mode assessment, performance and safety testing.
Maintains detailed documentation throughout all phases of research and development.
Reviews or coordinates outside vendor activities to support development.
Manages or coordinate technical solutions to design problems with vendors and in-house resources through design reviews, design audits and prototype analysis.
Interface with customers and internal departments articulating team activities and progress.
Work closely with manufacturing engineering to improve process, procedure, and cost.
Generate 3D models (Plastic & Sheet metal) & drawings using Creo / SolidWorks using any PLM/PDM tools.
Knowledge on Tolerance Stack-up Analysis, Validation documentation and GDT will be added advantage.
Understand the functional requirements of a product and ensure that the design changes meet the functional requirement.
Experience on create/ update FMEA documentation (PFMEA, DFMEA and Risk assessment)
Create and understand BOMs, routers and Inspection Plans according to requirements
May directly supervise one or more technicians or assemblers.
Candidate Desired Profile:
Bachelor’s in mechanical engineering with minimum 5 years’ experience in a related regulated medical device environment. Or a master’s degree with 2-3 years of related work experience, or an equivalent combination of education and work experience.
Hands on experience in SAP, Creo, SolidWorks, Engineering.
Ability to read and interpret documents such as safety rules, operating and maintenance instructions and procedure manuals; Ability to write routine reports and correspondence.
Ability to speak effectively before groups of customers or employees of organization, education, and experience.
Technical contribution through creative product design solutions that have been successfully launched into the market.
Ability to apply common sense, understanding to carry out instructions furnished in written, oral or diagram form; Ability to deal with problems involving a few concrete variables in standardized situations.
Values: Integrity, Accountability, Teamwork, Innovation

To apply for this job please visit careers.te.com.