Manufacturing Associate IV / V, Purification (Nights)

Role: Manufacturing Associate specializing in downstream (purification) processes in biopharma drug substance production. Responsibilities include executing cGMP manufacturing activities such as column chromatography, viral filtration, ultra-filtration, and bulk dispensing; operating process equipment; documenting data; and maintaining audit readiness. Requirements: Bachelor’s (preferably STEM) with 2+ years of experience or equivalent with relevant cGMP environment background; knowledge of aseptic/cleanroom protocols; familiarity with process automation systems (e.g., DeltaV, LIMS). Preferred: experience with pipetting and process validation. High-value specifics: biologics manufacturing in a GMP setting, focusing on downstream purification steps, in a 24/7 night shift schedule (2-2-3 rotation). Collaboration with production teams and adherence to high safety and quality standards are implied. Work setup: onsite in Research Triangle Park, with shift-specific hours.