GMP Manufacturing Technician

Pay Rate: Low: $25.00 | High: $31.00 Schedule: Monday – Friday, 8:00 AM – 5:00 PM Position: GMP Manufacturing Technician Job Summary The GMP Manufacturing Technician will support cell therapy manufacturing operations within the Advanced Cellular Therapeutics (ACT) Facility, a Good Manufacturing Practices (GMP) environment focused on the expansion, manipulation, and production of human cells for Phase I clinical applications, including CAR‑T cell therapies. This role involves hands‑on cell culture activities in an ISO7 cleanroom environment, following established Standard Operating Procedures (SOPs) to manufacture patient‑specific cellular therapy products while maintaining strict compliance with GMP standards. Key Responsibilities Perform cell culture and cell processing activities within an ISO7 cleanroom environment. Execute aseptic manufacturing techniques while working in Biological Safety Cabinets (BSCs). Follow GMP documentation, SOPs, and batch records to support manufacturing operations. Perform cell counting and assess manufacturing processes to support product quality and production decisions. Escalate questions, issues, or deviations appropriately and seek guidance when needed. Support inventory management, stocking, and organization of cleanroom materials and manufacturing supplies. Assist with the release and preparation of materials used in manufacturing operations. Participate in routine facility and manufacturing support activities as needed. Lead or assist with validation activities for manufacturing systems, equipment, and processes. Maintain compliance with GMP regulations, quality standards, and safety requirements. Qualifications Bachelor’s degree in Biology, Biotechnology, Cell Biology, Biochemistry, Biomedical Sciences, or a related scientific discipline required. Equivalent combination of education and relevant industry experience may be considered. Minimum of 3 years of relevant experience in GMP manufacturing, cell therapy, biotechnology, pharmaceutical manufacturing, or related regulated environments preferred. Experience working in cleanroom environments and following aseptic techniques. Familiarity with cell culture, cell counting, and biological manufacturing processes preferred. Strong attention to detail, documentation skills, and ability to follow SOPs. Ability to work independently while collaborating effectively within a manufacturing team. Preferred Experience Cell therapy, CAR‑T, gene therapy, or biologics manufacturing. GMP‑regulated manufacturing environments. Cleanroom gowning and aseptic processing. Equipment, process, or manufacturing validation activities. Batch record review and GMP documentation practices. This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you. #J-18808-Ljbffr Astrix Inc