Manufacturing Associate IV / V, Small Scale Purification (Days)

Role: Manufacturing Associate in biopharma drug substance production, focusing on downstream purification processes such as chromatography, viral filtration, and ultra-filtration. Objectives: execute daily cGMP manufacturing activities, ensure documentation accuracy, and maintain environment readiness. Responsibilities: operate process equipment, follow SOPs, perform in-process sampling, document deviations, and support validation activities. Requirements: Bachelor’s degree (STEM preferred) or equivalent experience (2-5 years), prior cGMP environment experience, familiarity with aseptic/cleanroom conditions, and understanding of process automation systems. Preferred: pipetting experience, exposure to single-use consumables. High-Value: biologics manufacturing, downstream process steps, cGMP compliance, and validation support in a 24/7 RTP facility. Work setup: day shift (6 AM–6 PM ET) on a 2-2-3 rotation; collaborative environment emphasizing training and safety.