Manufacturing Associate II / III, Purification (Days)

Role: Manufacturing Associate focused on downstream purification in biopharma drug substance production, operating in a cGMP environment. Responsibilities: execute processing steps such as column chromatography, viral filtration, ultra-filtration, and bulk dispensing; operate process equipment; document data and deviations; assist with sampling and analysis; maintain clean, audit-ready workspaces; contribute to team training and development. Requirements: Bachelor’s degree in STEM or equivalent, 0+ years of experience in GxP/cGMP manufacturing; knowledge of aseptic environments, SOPs, GDP, and process automation systems like DeltaV or LIMS; ability to follow procedures and work in a fast-paced, regulated setting. Preferred: experience pipetting, familiarity with cleanroom protocols. High-Value: biologic drug substance manufacturing, downstream processing, cGMP, sterile environments, 12-hour night shifts (2-2-3 rotation), Research Triangle Park location, entry-level to associate-level roles.