Biocompatibility/Reprocessing Engineer II

About the role

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™, QuikClot™, Rüsch™, UroLift™ and Weck™ – trusted brands united by a common sense of purpose. At Teleflex, we are empowering the future of healthcare.

Global Operations - Global Operations is a complex and diverse organization within the company which is responsible for product fulfilment to all our customers from end to end. We pride ourselves on being totally Customer Centric in our unrelenting focus on Improving Quality, Service and Value as perceived by our customers. Our employees are dedicated to the Global Operations Enterprise Excellence journey. Join a dynamic, growing team that offers healthcare providers an array of medical technology solutions that make a difference in patients’ lives.

Position Summary: Teleflex is seeking a Biocompatibility Engineer II to join our Global Biocompatibility department. The successful candidate will independently develop biocompatibility and reprocessing assessments and manage associated testing activities to support R&D, design and manufacturing changes, regulatory submissions, and other medical device projects. The Biocompatibility Engineer II will independently manage routine to moderately complex projects and apply scientific and engineering judgment to develop appropriate evaluation and testing strategies, with consultation from other subject matter experts as needed. This position is based at our Morrisville, NC office.

Expected Travel: Up to 10%

Responsibilities

• Independently author biocompatibility assessments and reprocessing assessments for assigned medical device projects in accordance with applicable procedures, standards, and regulatory requirements.
• Develop appropriate evaluation rationales and testing strategies based on available product, material, manufacturing, processing, historical, and testing information.
• Serve as