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™, QuikClot™, LMA™, Pilling™, 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.
• Responsible for project management, including the planning and implementation of program level project plans to facilitate full compliance with the new European Union Medical Device Regulation (EU MDR).
• Provide direction and understanding on the regulatory requirements of the MDR to functional leaders 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 management on a regular basis.
TRAVEL REQUIRED: 0-25% for team face to face
Principal Responsibilities• Develop, plan, communicate, and deploy project schedules. Responsible to meet project phase deliverables and milestones
• Maintain project schedule and tracking
• Lead cross-functional project team 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.
• Maintain project risk and issue log. 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.
• Minimum 3 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.
• Bachelor’s degree in a business or science discipline or equivalent education/experience is a plus.
• Knowledge and application of a disciplined project management process.
• Six Sigma and PMP certifications are a plus.
• Excellent written and oral communication, teamwork, and customer service skills among various departments and sites globally
• 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
• Attentive to detail and analytical decision-making required
• Regulatory Affairs, EU MDR, or project management experience required
• Ability to prioritize projects and adapt to shifting priorities
Teleflex is an equal opportunity employer. Applicants will be considered without regard to age, gender, race, nationality, ethnicity, civil status, family status, sexual orientation, disability, religion and/or membership of the traveller community.
If you require accommodation and support to apply for a position, please contact us at talent.emea@teleflex.com.
Diversity fosters innovative thinking and entrepreneurship and that’s what we are about at Teleflex. We trust and value our people and their diversity and we make it fun to work here. We are on a journey to ensure our workplaces mirror the patients we serve and the communities we operate in. Our approach is simple, we embrace everyone and want them to feel they belong here. We are building a culture where all employees can bring their best and unique selves to work. If that appeals to you, we would love to hear from you. Come join a company where diversity is sought out and inclusivity is how we progress.
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™, QuikClot™, LMA™, Pilling™, Rüsch™, UroLift™ and Weck™ are trademarks or registered trademarks of Teleflex Incorporated or its affiliates, in the U.S. and/or other countries.
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