Position will also be responsible for performing downstream processing activities, including chromatography, ultrafiltration/diafiltration (UF/DF), buffer preparation, filter integrity testing, and manual and/or automated filling of viral vector material. Position will also be collaborating with manufacturing, MSAT, Facilities & Engineering, and Quality teams to support GMP production runs, troubleshoot/escalate equipment or process issues, and assist with revisions to SOPs, MPRs, and other controlled documents.