Manufacturing Associate III / IV, Purification (Nights)

Role: Manufacturing Associate focused on downstream purification in biopharmaceutical drug substance production. Responsibilities: perform processing steps such as column chromatography, viral filtration, ultra-filtration, and bulk dispensing; operate process equipment; document activities per cGMP SOPs; maintain clean and compliant work environment; collaborate cross-functionally with Manufacturing, MSAT, Quality, and Engineering teams. Requirements: Bachelor's degree (STEM preferred) with 0.5+ years or relevant experience in a cGMP environment; understanding of aseptic/cleanroom processes; familiarity with process automation (e.g., DeltaV, LIMS); pipetting experience preferred. Experience levels vary by role (Associate III or IV). High-Value: biologics manufacturing, drug substance, cGMP compliance, downstream purification, validation protocols, cleanroom environment. Work setup: night shift (6 PM – 6 AM ET), 2-2-3 calendar rotation, onsite at RTP.