Manufacturing Associate III / IV, Purification (Nights)

Role: Manufacturing Associate specialized in downstream bioprocessing (purification) within a cGMP environment, supporting biologics production at Biogen's RTP facility. Responsibilities: execute and document daily manufacturing activities including operation of chromatography, viral filtration, ultra-filtration, and bulk dispensing; perform in-process sampling and analysis; maintain audit readiness and a safe work environment; contribute to documentation updates and team training. Requirements: Bachelor's degree in STEM with 0.5+ years or an associate's degree with 1+ year of relevant experience in a cGMP setting; familiarity with SOPs, GDP, aseptic/cleanroom environments, and process automation systems (e.g., DeltaV, LIMS); pipetting experience preferred. High-Value: biologics manufacturing, cell culture/downstream processing, cGMP compliance, validation protocols, and experience working with biotech manufacturing equipment. Work Setup: night shift (6:00 PM–6:00 AM ET), rotating 2-2-3 schedule, in RTP; no specific travel requirements stated.