Manufacturing Technician

Our client is a leading pharmaceutical company specializing in the development and manufacturing of innovative drug delivery systems. They are seeking a detail-oriented Manufacturing Technician to support GMP manufacturing and packaging operations at their Minnesota facility. This onsite role requires hands-on experience in pharmaceutical or medical device manufacturing, with a strong emphasis on quality documentation and cGMP compliance. Essential Functions and Responsibilities Responsible for quality of products and documentation; adheres to all manufacturing process and quality requirements Receives and distributes materials and supplies in the manufacturing area Works with manual and automated equipment to complete assembly, final packaging, and inspection of pharmaceutical products Moves materials within the production area Responsible for maintaining uninterrupted loading/unloading of materials and assembled devices from multiple stations of an automated assembly process Interacts with automated equipment to perform basic fault resetting, monitoring of material inputs/outputs, and entering setup/run information Completes assigned training prior to due dates Assembles products following all current Standard Operating Procedures (SOPs) and Work Instructions (WIs), while meeting manufacturing goals and metrics Maintains accurate records following Good Documentation Practices (GDP) and cGMP guidelines, including training files and shop floor paperwork Other duties as assigned Education and Experience High School Diploma or equivalent required Minimum 1 year of experience in a medical and/or pharmaceutical manufacturing setting An equivalent combination of experience and education may be considered Knowledge and Skills Critical understanding of the importance of documentation and data traceability Ability to work safely and responsibly in a fast-paced manufacturing environment Familiarity with executing Standard Operating Procedures (SOPs) in a manufacturing or assembly environment, preferably in the pharmaceutical industry Demonstrates strict attention to detail Basic computer skills (Microsoft 365) Working knowledge of Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP) preferred Ability to work well both independently and in a team environment Excellent verbal and written communication skills Strong organizational and multi-tasking skills Must be able to work in a controlled or clean room environment requiring special gowning Ability to perform physical activity including standing for long periods, walking, and manual work; may require lifting up to 30 lbs. #J-18808-Ljbffr Hydrogen Group