Senior Engineer, Software Development

Expected Travel: Up to 10%

Requisition ID: 12993

 

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™, QuikClot™, Rüsch™, UroLift™ 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 teleflex.com.

 

Vascular Access – Built on a history of innovation, our Arrow™ brand of technically advanced vascular access devices are renowned throughout the world. Many of our vascular access products have antimicrobial and antithrombogenic protection designed to reduce vascular-related complications and include long and short dwell central venous catheters (CVC), sheath introducers, arterial lines, peripherally inserted central catheters (PICC), as well as specialty devices and an advanced vascular positioning system to facilitate precise placement of a PICC or CVC near the heart. Join a dynamic, growing team that offers healthcare providers an array of medical technology solutions that make a difference in patients’ lives.

Position Summary

At Teleflex, we are committed to empowering the future of healthcare.

As a Senior Engineer specializing in Software, you will be instrumental in implementing technological innovations in vascular positioning systems, including artificial intelligence/machine learning (AI/ML), application software, and embedded software systems. This role involves providing strategic cross-functional technical leadership to ensure alignment with best practices and frameworks for delivering high-quality software solutions. You will be responsible for reinforcing software excellence and achieving reliable and predictable software market releases.

Principal Responsibilities

1.    Designs, develops, verifies, and maintains medical device software following industry best practices, ensuring scalability, reliability, and maintainability of software systems for connected medical systems.
2.    Partakes in design control activities and documentation efforts, including requirements, risk assessments and mitigation, traceability, V&V protocols and reports, coding reviews, and software releases.
3.    Collaborates with stakeholders, third-party designers, vendors, and contractors to deliver high-quality engineering solutions.
4.    Participates in risk assessments and failure mode analysis (FMEA) to identify and mitigate potential risks.
5.    Comfortable with all layers of full-stack development and verification of medical devices, while ensuring compliance with all relevant regulations.
6.    Defines, develops, and maintains automation at all levels of the software stack as it relates to DevOps, release management, and CI/CD pipelines.
7.    Participates in all SDLC activities and maintains relevant, accurate and complete documentation.
8.    Complies with Teleflex’s code of Ethics, the company’s Quality System, and all company policies, rules, and housekeeping standards.

Education / Experience Requirements

•    Master’s Degree in Computer Science or equivalent with appropriate experience (Computer Engineering, Electrical Engineering).
•    8+ years of software development in senior development or lead roles, preferably in medical devices or regulated industry, with experience in deployment of commercial products.
•    Highly motivated to share knowledge and mentor others.
•    Hands-on experience with multiple operating systems (Windows, iOS, Android), scripting and programming languages (PowerShell, C#), programming paradigms (OO, concurrent, declarative), cloud computing (Azure), YAML, Azure DevOps, CI/CD, SCM, Git, Verification Automation, Agile, Scrum, and SDLC preferably in a regulated environment (medical devices, automotive, aviation).

Specialized Skills / Other Requirements

•    Experience with medical device regulatory standards such as 21 CFR Part 820, IEC 60601, IEC 62304, and ISO 13485, including experience with system risk, hazard analysis, and DFMEA.
•    Deep commitment to understanding and solving problems for end users, with an ability to translate into software requirements, design, and test specifications.
•    Track record of cross-functiona