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Job Description
Complaint Reporting MDR/Vigilance Specialist 2 Teleflex - 3.7 Morrisville, NC Job Details 10 hours ago Qualifications Microsoft Word FDA submissions Nursing Microsoft Excel Microsoft Outlook Adverse event reporting Bachelor of Science Bachelor's degree in biomedical engineering Regulatory reporting Biomedical Engineering Complaint handling Mid-level Key Performance Indicators Bachelor's degree Continuous improvement Task prioritization Risk management Bachelor's degree in nursing Regulatory submissions Quality systems 1 year Training Communication skills
ISO 13485
Time management
Full Job Description Date:
Apr 30, 2026
Location:
Morrisville, NC, US Company:
Teleflex Expected Travel :
Up to 10%
Requisition ID :
13762 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 Work within Complaint Intake & Reporting team to critically review complaints to determine reportability based on the regulatory requirements, risk documentation and clinical experience. Responsible for preparation and timely submissions of MDR/Vigilance reports to FDA/Competent Authorities and other regulatory agencies. Where necessary, seek and document relevant additional information in line with the complaint intake process. Identify potential issues to continuously improve process. Principal Responsibilities Utilizes clinical experience in conjunction with risk management documentation to review complaints for adverse event reportability in accordance with US Canadian & European regulations within required time frames. Follows up with health care providers and customers to provide clarification for complaint files and document correspondence to complaint files as required. Prepare and submit regulatory reporting documentation such as MedWatch forms with FDA and Vigilance Reports with Canadian and European regulatory authorities. Assist as clinical liaison for the complaint management department to facilitate understanding of clinical application for product complaint devices and provide training to other team members as required. Utilize complaint management system to accurately document complaint information. Final Reviewer/Approval of reporting decisions and initial reports Support audit activities are required. Assists with responses to FDA and Competent Authority for additional information queries. Work to meet team KPI's Department Metrics and over QA/RA goals and objectives. Support improvement projects in the complaint intake and reporting function. Support wider QMS and risk management activity as required.
Education / Experience
Requirements B.S. Degree in Nursing, Biomedical Engineering, or related science discipline 1-3 years medical device experience Experience in Post-Market Surveillance with a preference for experience in Complaint Handling/Vigilance Reporting. Demonstrated knowledge of Medical Device Quality Systems regulations, including FDA's 21 CFR 820, 21 CFR 803, ISO 13485:2016, MDD, EU
MDR, MDSAP.
Specialized Skills / Other Requirements Ability to critically review information and seek clarification. Ability to work well under deadlines and pressure in a changing environment. Skilled in use of Microsoft suite of applications i.e., Excel, Outlook, and Word. The ability to prioritize tasks and manage several tasks simultaneously. Ability to read understand and self-educate on emerging regulatory requirements.
