Expected Travel: None

Requisition ID: 13335

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.

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

Responsible for project management, including the planning and implementation for their specificTeleflex Business Unit, to facilitate full compliance with the new European Union Medical Device Regulation (EU MDR).

Will provide direction and understanding on the regulatory requirements of the MDRto the BU RAas well as responsible to influence a wide range of functions and departments to drive the project's strategic initiatives while managing tactical activities and partnering effectively with a large and varied group of stakeholders. Collaboration with shared services partners to ensure effective planning and delivery of requirements to meet product compliance deadlines.

Ensure team commitments (scope, schedule and budget) are met. Communicate project status to Snr Project Manager on a regular basis.

Principal Responsibilities

Develop, plan, communicate and deploy project schedules. Responsible to meet project phase deliverables and milestones
Maintain project governance
Partner with MDR Business Unit Lead and Team regarding common interpretation and guidance, deliverables, pace and progress to ensure a harmonized approach for achieving compliance
Collaborate with project team, business units, and workstream/shared services leads, as well as functional leaders from regulatory, quality and clinical functions to finance, R&D and operations to ensure efficient execution of a shared strategy
Ensure overall compliance; promote creative solutions; ensure on-time completion of individual tasks and project workstream goals
Support the development of harmonized business processes and procedures for execution and compliance with EU MDR
Communicate effectively with program leadership to ensure clear expectations, demonstrate progress and identify issues. Provide progress updates and regular reporting to business and functions leadership
Through the implementation of project management and productivity tools, maintain and track progress and produce applicable reports
Partner with other project leaders to ensure coordination of activities and timelines, facilitating efficient use of resources
Partner with Regulatory and Quality Operations as well as IT project management to develop systems and IT tools requirements to support effective standard processes
Facilitate regularly scheduled meetings, take meeting minutes with action items, and follow up with SMEs on expected deliverables.

Education / Experience Requirements

Bachelor's degree in a business or science discipline or equivalent education/experience required.
Minimum 2 years project management experience in the medical device and/or FDA regulated industry.
Minimum 5 years project management experience in large organizations with national or global operations.
Knowledge and application of a disciplined project management process.
Six Sigma and PMP certifications a plus.

Specialized Skills / Other Requirements

Must have Regulatory Affairs experience/knowledge and relevant experience in project management and process improvement skills.
Strong influence management skills. Demonstrated ability to work cooperatively at all levels in a matrix organization to build and maintain the positive relationships required to accomplish project goals
Excellent verbal/ written communication and presentation skills. Demonstrated ability to succinctly and accurately communicate to various levels of management and across the organization
Ability to support multiple projects and balance priorities, work independently or collaboratively to determine and develop solutions
MS Project, Excel, PowerPoint, SharePoint
Exceptional facilitation, analytical, planning, organization and time management skills to effectively execute project plans
Excellent decision-making skills. Ability to negotiate and balance decisions and manage competing priorities across multiple functional areas

Note: As with all positions, due to the dynamic nature of Teleflex Medical business, key responsibilities may evolve and change over time.

Teleflex is an equal opportunities employer.

At Teleflex, we follow a comprehensive hiring process. We do not accept unsolicited resumes from agency recruiters or 3rd party firms. We do not make unsolicited job offers. We do not ask for money or require equipment purchase up-front.

Teleflex, the Teleflex logo, Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ are trademarks or registered trademarks of Teleflex Incorporated or its affiliates, in the U.S. and/or other countries.

© 2026 Teleflex Incorporated. All rights reserved.

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