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

Role: Manufacturing Associate focusing on downstream (purification) processes in biopharma drug substance production at RTP, supporting 24/7 cGMP operations. Responsibilities include operating process equipment such as chromatography, viral filtration, and ultra-filtration, executing validation protocols, documenting cGMP data, preparing batch records, assisting with in-process sampling, and maintaining a clean, audit-ready environment. Requirements: for Associate III, a minimum of 0.5-1.5 years of relevant experience, with a STEM degree, BioWorks certificate, or high school diploma, and prior cGMP environment experience; for Associate IV, 2-3+ years, with similar qualifications. Skills include adherence to SOPs, good documentation practices, aseptic environment experience, process automation understanding (e.g., DeltaV, LIMS), and pipetting skills; exposure to single-use consumables preferred for IV. High-Value: biologics manufacturing, cell culture processing, cGMP compliance, validation, cleanroom environment, and downstream bioprocessing. Work setup: day shift (6 AM–6 PM ET), rotating 2-2-3 schedule, in RTP, with potential to progress in biomanufacturing career.