TE Connectivity Senior Design Engineer in Galway, Ireland
TE Connectivity (NYSE: TEL) is a $12 billion global technology leader. Our connectivity and sensor solutions are essential in today’s increasingly connected world. We collaborate with engineers to transform their concepts into creations – redefining what’s possible using intelligent, efficient and high-performing TE products and solutions proven in harsh environments. Our 72,000 people, including over 7,000 engineers, partner with customers in over 150 countries across a wide range of industries. We believe EVERY CONNECTION COUNTS – www.TE.com.
Senior Design Engineer
Primary Objectives of Position:
As part of the Design Engineering team at our Parkmore facility the Senior Design Engineer will lead and be an integral part of a team developing Creganna's portfolio of platform delivery system products. This position requires a candidate with significant product development experience in the medical device arena, and one who will be comfortable leading and developing a team to develop Creganna’s products. She/he will report to the Group Leader, and the position will be based in our Parkmore facility.
Lead and be an integral part of the team tasked with the development process from concept generation through to design verification.
Assist in the development of intellectual property generated by development activities.
Ensure the application of new and existing technologies to provide the optimum delivery system design.
Participate in trials with physicians to provide clinically relevant feedback on product designs.
Provide technical feedback during frequent technical contact with customers to optimise product design.
Support the maintenance of product files and other relevant documentation to comply with quality standards.
Compile project plans and lead team to develop devices in accordance with planned activities, budget and timelines.
An engineering, science or equivalent degree.
5 to 8 year’s industry experience in a medical product development environment with a proven track record of leading teams in device development.
Experience of coordinating and leading Design Reviews and the compilation of associated documentation.
Leading the team to carry out actions in accordance with the project plan and deliver projects through key milestone phases and associated activities.
Demonstrate a thorough knowledge and understanding of ISO 13485 & FDA 21 CFR Part 820 Design Control requirements.
Proven experience of minimally invasive Medical Device design, development and manufacturing.
Proven experience in leading teams performing FMEA’s, verifications and validations for medical devices products and processes. Knowledge and experience with Medical Device sterilisation processes, specifically gamma and EtO sterilisation.
Proven experience of work with catheter technology, catheter design and testing and catheter manufacturing a distinct advantage.
Experience with engineering tools such as DOE, SPC, and using Minitab
3D modeling experience.
Working knowledge of biocompatible metal and/or polymer materials.
Demonstrate a working knowledge of the required activities and deliverables from each of the development phases.
Availability to participate in limited travelling to meet with customers to conduct scheduled reviews.
Requisition ID: 2017-82095
Business Unit (Current): Industrial Solutions - Medical - Creganna Medical
External Company URL: www.tycoelectronics.com