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Job Description
Date:
Jun 25, 2026
Location:
Maple Grove, MN, US #job-location.job-location-inline { display: inline; }
Company:
Teleflex Expected Travel:
None Requisition ID:
14018 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 Teleflex is seeking a Document Control Specialist to join our Quality department. The successful candidate will be responsible for reviewing batch records, work orders, and overall data generated for Blood Products. Strong attention to detail and understanding of GMP regulations are necessary for this position. This position is based at our 6420 Sycamore Ln N, Maple Grove, MN 55369 office. Principal Responsibilities Verifies data and results are accurate prior to batch disposition. Verifies all equipment is compliant for use (ensuring equipment is within calibration). Verifies all reagents, standards, and solutions used during testing were prepared correctly and compliantly. Responsible for collaborating with other departments to resolve documentation issues. Responsible for ensuring cGMP requirements are being followed. Responsible for communicating atypical and OOS results to laboratory management. Adhere to and ensure compliance with the Teleflex Code of Ethics, all company policies, rules, and procedures. Complete other duties and tasks as assigned.