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Production Operator II

Job in Maple Grove, Hennepin County, Minnesota, 55311, USA
Listing for: Teleflex
Full Time position
Listed on 2026-09-10
Job specializations:
  • Manufacturing / Production
    Medical Device Industry, Production Associate / Production Line, Manufacturing & Industrial Operations, Quality Engineering
Salary/Wage Range or Industry Benchmark: 20.38 - 28.55 USD Hourly USD 20.38 28.55 HOUR
Job Description & How to Apply Below

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Expected Travel: None
Requisition : 14378

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™, Quik Clot™, Rüsch™, Uro Lift™ 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

Vascular & Emergency Medicine - Built on a legacy of innovation and clinical excellence, the Vascular & Emergency Medicine business at Teleflex develops and delivers advanced medical technologies that empower clinicians to help improve patient outcomes and optimize healthcare efficiency. Our trusted Arrow™, Arrow™, EZ-IO™, and Quik Clot™ brands set the standard for vascular access and emergency medicine, offering proven solutions to enhance patient outcomes.

From technically advanced vascular access devices - including central venous and arterial catheters, PICCs, and sheath introducers with antimicrobial protection-to life-saving intraosseous access systems and hemostatic technologies used by hospitals, EMS, and military teams worldwide, our portfolio embodies precision, reliability, and performance. As part of a high-performing, purpose-driven organization, we are united by a commitment to clinical differentiation, innovation, and excellence.

Join a dynamic, growth-focused team that offers advanced medical technology solutions that make a lasting impact on healthcare.

Position Summary

Manufacture, process, inspect, document, and package freeze-dried plasma products in a controlled cleanroom environment. Operate production equipment used to thaw, transfer, lyophilize, and package plasma while maintaining product traceability and complying with current Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), approved procedures, and safety requirements. Support production readiness and continuous improvement through procedure review, accurate documentation, and authorized redlining of production procedures.

  • Champion a safety-driven culture and comply with applicable safety, environmental, and occupational health requirements.
  • Manufacture, process, inspect, and package product in accordance with approved procedures, production records, and established quality requirements.
  • Perform plasma-processing activities, which may include retrieving frozen plasma, operating thawing equipment, transferring liquid plasma, loading and unloading lyophilization equipment, and repackaging finished product.
  • Operate applicable production equipment, including balances/scales, bag sealers, thawers, hoods, lyophilizers, computers, label printers, and glove boxes, after required training and qualification.
  • Complete visual, dimensional, time, label, and documentation checks accurately and within established production standards.
  • Maintain complete and accurate product traceability and production records, including timely data entry in the BECS system or other approved systems.
  • Identify and promptly report quality issues, process deviations, equipment concerns, material defects, or workmanship deficiencies in accordance with established procedures.
  • Comply with GMP and GDP requirements, maintain required training records,…
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