Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.
Job Description
Director, Quality Management Systems Teleflex - 3.7 Morrisville, NC Job Details 21 hours ago Qualifications Regulatory inspections Preventive action implementation Compliance audits & assessments Quality control preventive actions Corrective and preventive actions (CAPA) Team development Quality risk management Project management in healthcare Mentoring Biomedical regulatory compliance Managing projects Quality audits Project stakeholder communication Cross-functional communication Stakeholder management
Full Job Description Date:
Jun 26, 2026
Location:
Morrisville, NC, US #job-location.job-location-inline { display: inline; }
Company:
Teleflex Expected Travel:
Up to 10%
Requisition ID:
14026 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 This position reports to the Sr Director, Quality Excellence & Systems. Improve and maintain the global Quality System in line with ISO 13485, Medical Device Directive (MDD), Medical Device Regulation (EU-MDR), MDSAP International Regulations (Australia, Brazil, Canada, Japan, USA) and regulatory requirements applicable to the Quality Management System (QMS). The role will also involve multi-site collaboration with various facilities and departments. Provide regular status reports to management as required. As a People Manager, you play a pivotal role in leading, developing, and inspiring a high-performing team to deliver exceptional results aligned with organizational goals. You are responsible for building organizational capability through effective talent development, fostering a culture of accountability, and promoting continuous improvement. Your role requires strong cross-functional collaboration to ensure alignment and drive integrated solutions across the business. As a leader, you are a visible champion of our culture and values, creating an inclusive, purpose-driven environment where individuals feel empowered to contribute and grow. Principal Responsibilities
PRINCIPAL RESPONSIBILITIES
Plan and manage the duplication and certification of the QMS during the divestiture Own and liaise with eQMS vendor, systems team, and global process owners to manage divestiture and subsequent system integrations (e.g., PLM, ERP) as needed Direct facilities (Athlone, Morrisville, Pleasanton, Santa Barbara, and others as assigned) and their Quality Management Representatives and ensure the QMS is consistently established, implemented, and maintained Partner with Regulatory Affairs and communicate with Notified Bodies and regulators with respect to certificates, audits, and QMS elements as necessary Support quality system and regulatory audits including by not limited to FDA, Notified Body
ISO 13485/MDSAP/EU
MDR, Customer and Internal audits Develop, implement and monitor key metrics used to assess Quality System Execution Support change control activities including reviewing and approving QMS documentation, supporting impact assessment, and attending technical reviews to provide feedback on QMS processes Develop, enact, and maintain the global QMS certificate strategy for the enterprise Ensure alignment between the Global QMS and facilities' local QMS Ensure consistency between the design center QMS and activities Lead Strategic QA Projects Establish function-specific quality objectives, create quality planning documentation when necessary, and lead a continuous monitoring process for the facilities based on inputs from relevant stakeholders Manage budgetary requirements and ensure compliance of expenditures to meet the budget Build interdependent relationships with R D, Marketing, Operations and RA and Administration Support the Global Corrective Action and Preventive Action (CAPA) program by reviewing and approving Global Quality Management System CAPAs and participating in the executive CAPA Review Board (eCRB) as the Quality Management Systems representative Participate in mergers and acquisitions, providing due diligence and Quality support Support and lead additional activities as assigned by Sr. Director, Quality Excellence & Systems or Executive Leadership Education / Experience Requirements Bachelor of Science (preferred in Engineering, Microbiology or other technical degree) Experience Managing the Quality Management Systems and medical device regulations Experience with regulatory inspections/audits Experience with Project Management Experience and knowledge of process risk management and CAPA systems Excellent organizational skills Excellent written and verbal communication skills Excellent stakeholder management skills Specialized Skills / Other Requirements
