Manufacturing Associate IV

About This Role:Manufacturing Associates in Oligonucleoitide Synthesis (OSM) perform and document daily manufacturing operations in a cGMP environment. This involves operation of process equipment, execution of validation protocols, creating/revising cGMP documents and other assignmentsWhat You’ll Do:Execute manufacturing processing steps and/or manufacturing support activities, monitoring the process against the batch record and control system. May coordinate or lead process steps as requested.Document/Record and Review cGMP data and information (including documentation of deviations) for processing steps and/or equipment activities, following standard operating procedures. Revises or creates documents as instructed. Key documentation includes batch records, SLRs, and equipment logbooks.Actively participates in training activities, managing their individual training plan. Trains other associates as required.Executes validation protocols with minimal supervision/direction of others.Who You Are:You enjoy being a part of a high performing team that is agile in its ability to meet its production schedule.  You also like being accountable in driving tasks and projects to completion while getting exposure to responsibilities supporting the manufacturing process