Upstream Manufacturing Associate II

Pay range: 25-35/hr depending on experience Position Overview The Upstream Manufacturing Associate II independently executes upstream manufacturing operations in a cGMP cleanroom environment. This role requires technical expertise in mammalian cell culture, bioreactor operations, harvest processing, and in-process testing while serving as a mentor to junior associates and supporting process improvements. Key Responsibilities Upstream Manufacturing Operations Independently execute media and buffer preparation activities. Perform cell culture expansion, vial thaw, seed train operations, and production-scale bioreactor processing. Operate and monitor fed-batch and perfusion bioreactor systems. Execute harvest, filtration, and process transfer operations. Troubleshoot manufacturing and equipment issues within established procedures. In-Process Monitoring Perform routine process monitoring and data review. Operate analytical equipment including: Cedex Cell Analyzer Blood Gas Analyzer (BGA) Osmometer pH and conductivity meters Aseptic Processing & Compliance Perform aseptic operations in classified environments. Maintain GMP-compliant documentation. Participate in deviation investigations and root cause assessments. Support audit preparation and inspection activities. Training & Continuous Improvement Train and mentor Associate I personnel. Assist with SOP revisions and manufacturing documentation updates. Participate in process improvement and operational excellence initiatives. Support technology transfer and manufacturing readiness activities. Qualifications Education & Experience Bachelor’s degree in Biotechnology, Biochemistry, Chemical Engineering, Life Sciences, or a related discipline with 3-5 years of relevant biopharmaceutical manufacturing experience. High School Diploma/GED with 6+ years of relevant experience may be considered. Required Skills Strong understanding of mammalian cell culture and upstream processing. Experience operating bioreactors and associated equipment. Knowledge of GMP manufacturing requirements. Strong analytical and troubleshooting skills. Effective communication and team collaboration abilities. Preferred Skills Experience with: Single-use bioreactor systems Perfusion technologies Cell culture analytics Process troubleshooting Technology transfer activities Physical Requirements Ability to stand for extended periods. Ability to bend, reach, and lift up to 50 pounds. Ability to work in cleanroom environments while wearing required PPE. #J-18808-Ljbffr Planet Pharma