Manufacturing Associate (Pharma)

Looking for potentially 2 people. Role(s) will begin with working in the kitting and labeling department, packaging and labeling 2-30mL vials. Someone with 1 year of experience with Good Document Practices would be ideal so that they have a basic understanding. As the role evolves and based on performance, tehre will be opoetunities to move into higher level positions within manufacturing, and/or move to 3rd shift. There are built in pay increases for both 3rd shift and becoming gown qualified. Plenty of overtime will be available, but is not mandatory. Standard shift begins at 7:30AM for a daily meeting, and will end at 4PM, Monday through Friday.

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Responsible for participating in upstream and/or downstream aseptic manufacturing of LAL products in a ISO 5 environment according to company and departmental SOPs. Performs set-up and operate production equipment in the LAL Filling and Finishing areas. Performs product inspections and final kit packaging of finished goods.
Operating in a safe work culture (safety chats, safety and EPS observations, 6S)Completion of LAL Cleanroom General TrainingAseptic processing/gowningCleanroom Equipment Set-Up and UsageEnvironmental MonitoringQualification of SAP Transactions (COR3, COR6, MIGO, LS26)Completion of LAL Finishing General TrainingFinishing Equipment Set-Up and UsageQualification of SAP Transactions (COR2, COR6, MIGO, MB1A, LB01, LS26)GMP Documentation practicesProduct Sample SubmissionInspection Proficiency TestingInspection ProcessComponent Kitting ProcessContinuous Improvement ProjectsPerform job functions with minimal operator related PRsPerform aseptic processing with minimal xzbcwsv operator related personnel excursions (EM)Understand basic level of LAL process flowAchieve yearly personnel utilization targetMaintain training compliance to meet yearly targetMust be able to demonstrate GMP documentation practices (minimal document errors)Must be able to follow standard operating procedures and complete production recordsUnderstand compliance in the execution of GMPs in a manufacturing environmentComply with all safety policies and general regulationsPerform other duties as assigned