**Date**:May 5, 2025 **Location**: Bogotá, DC, CO **Company**:Teleflex **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. **Latin America -** The Latin America Region of Teleflex is headquartered in Morrisville, North Carolina, and supports our customers, distributors, sales managers and specialists in Mexico, Brazil, Colombia, Chile, Argentina and Puerto Rico. The Latin America Region sells a broad spectrum of medical devices and related products in the fields of vascular and interventional access, surgical, anesthesia, cardiac care, urology, emergency medicine and respiratory care. As Teleflex grows and expands its portfolio, we will continue to grow our presence in Latin America. Join a dynamic, growing team that offers healthcare providers an array of medical technology solutions that make a difference in patients’ lives. **Position Summary** The Quality Assurance Specialist will support Quality System elements for Teleflex Logistics and Distribution centers within Colombia that support Labeling, Document Control and Quality Systems Training in accordance with internal procedures and external regulations and standards. Also will establish metrics, analyze, trend and report on employee training compliance data, labeling KPI’s and document control metrics, as well as give support for global projects impacting operations within L&D.; **Principal Responsibilities** - Supports global activities related to product, including resolution of regulatory and quality issues. - Serves on Regional and Corporate level teams as assigned. - Suggests and debates alternative methods and procedures in solving problems and meeting changing related to importation, storage, distribution and commercialization. - Develops initial and subsequent modifications of product assurance program to delineate areas of responsibility, personnel requirements, and operational procedures within program. - Evaluates contents of reports from quality assurance initiatives and confers with management personnel preparatory to revisions to product assurance program. - Reviews procedures of departments and recommends solutions to problems or changes in procedures. - Confers with representatives of material and component vendors to obtain information related to supply quality, capacity of vendor to meet orders, and vendor quality standards. - Confers with Teleflex Manufacturing sites about quality assurance aspects of manufactured products. - Reviews technical publications, articles, and abstracts to stay abreast of technical developments in industry. - Coordinates and facilitates customer, corporate compliance, and regulatory/registration audit visits. - Prepares and submits required corporate reports relative to quality reporting, and general regulatory compliance. - Maintains the internal audit system. - Maintains the calibration program of all measuring and test equipment used to accept product. - Oversees and ensures the documentation system is in place and effective for assigned sites. - Provides support to the evaluation and quoting of new business opportunities via project and specification review, project and costing analysis and associated negotiations with new and existing customers. - Technical Responsible before INVIMA. - Vigilance contact before INVIMA regarding field actions and product complaints. - Manage the labeling database for nationalization labels. - Prepares and updates “fichas técnicas” for registered products in Colombia. - Organize and administer a database of quality information required including but not limited to product complaints, field actions, non-conformances, ship holds, and management control changes. - Develop and updates as necessary, the procedures for Teleflex Medical Colombia SAS. - Ensure that regulations required for commercialization are met, such as but not limited to reviwing procedures of medical equipment after importation and prior to commercialization, and nationalization labelling. - Maintain the quality system (documents and activities) and constantly improve the process involved - Liaison between the warehouse and Teleflex Medical Colombia SAS in relation to ship holds including restriction and disposition of local product. - Communicate any significant or potential significant quality issues caused or received by the warehouse such as bu