Engineer , Sustaining, R&D
Job in
Morrisville, Wake County, North Carolina, 27560, USA
Listed on 2026-07-26
Listing for:
Teleflex
Full Time
position Listed on 2026-07-26
Job specializations:
-
Engineering
Systems Engineer, Biomedical Engineer, Medical Device Industry, Quality Engineering
Job Description & How to Apply Below
Expected Travel:
Up to 10%
Requisition
About Teleflex Incorporated
As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people's lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We believe that the potential of great people, purpose-driven innovation, and world-class products can shape the future direction of healthcare.
Teleflex is the home of Arrow, Barrigel, Deknatel, LMA, Pilling, Quik Clot, Rüsch, Uro Lift and Weck - trusted brands united by a common sense of purpose.
At Teleflex, we are empowering the future of healthcare. For more information, please visit
Vascular & Emergency Medicine - Built on a legacy of innovation and clinical excellence, the Vascular & Emergency Medicine business at Teleflex develops and delivers advanced medical technologies that empower clinicians to help improve patient outcomes and optimize healthcare efficiency. Our trusted Arrow, Arrow, EZ-IO, and Quik Clot brands set the standard for vascular access and emergency medicine, offering proven solutions to enhance patient outcomes.
From technically advanced vascular access devices - including central venous and arterial catheters, PICCs, and sheath introducers with antimicrobial protection-to life-saving intraosseous access systems and hemostatic technologies used by hospitals, EMS, and military teams worldwide, our portfolio embodies precision, reliability, and performance. As part of a high-performing, purpose-driven organization, we are united by a commitment to clinical differentiation, innovation, and excellence.
Join a dynamic, growth-focused team that offers advanced medical technology solutions that make a lasting impact on healthcare.
Position Summary
Under general direction, the Sustaining R&D Engineer, based in Morrisville NC, is responsible for the sustaining engineering projects of Anesthesia and Emergency medicine products. Experience and background requirements should focus on disposable medical device products. This position has PTG (Product Technology Group) responsibility, including organizing and managing multiple projects and ensuring they are completed in a timely manner. Assignments will primarily be focused on existing products within the portfolio, providing creative solutions to technical issues or modifying/improving the product as required.
The candidate must be capable of advanced level scope of assignments in planning, designing, and coordinating the development and implementation of related engineering activities to support changes and improvements to existing products lines, and implement successfully into manufacturing. Incumbent at this level self-manages their project work, seeks help when required, and is fully aware of the operating procedures and policies of the work unit
Principal Responsibilities
* Acts as product technology group owner/subject matter expert for assigned product lines.
* Coordinates the product design and development process with appropriate support departments such as engineering, quality, regulatory, marketing, documentation, operations, procurement.
* Serve as an R&D technical lead representative in transfer, integration, or other corporate initiative core teams. Collaborate with Engineering, Quality, and Regulatory to understand technical targets and design control systems.
* Serves as project leader for assigned projects; responsible to follow up on all aspects of projects. Reports project statuses and key metrics and dashboard updates to required systems.
* Resolves complex process/product development and manufacturing issues; independently takes lead of working cross functional teams.
* Prepares formal documentation of the product designs, change management, risk analysis, product requirements and specifications, customer needs, etc. according to established product development procedures. Initiates formal reviews to progress projects to compliant completion.
* Prepares or coordinates development of design drawings, specifications, estimates of costs, documentation updates, etc. Utilizes appropriate PLM, ERP and other product-related database systems.
* Conducts research on projects associated with the design and/or design modifications of medical devices, components, models, or mechanisms.
* Develops, maintains, and publishes plans for assigned projects with critical milestones and timelines. Owns the change management activities for sustaining or supplier-initiated changes. Leads design transfer activities when required.
* Develops and coordinates the execution of protocols for validations of new or modified devices or components, including validations of the design, test methods, manufacturing processes, assembly, packaging, and sterilization where applicable.
* Primary R&D interface with operations for cost…
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