Associate Manufacturing - Thousand Oaks CA

Associate ManufacturingLet's do this. Let's change the world. In this dynamic role you will collaborate with multiple functions within the Thousand Oaks site on a routine basis in a dynamic environment (Quality Assurance, Quality Control, Engineering, Facilities, Maintenance, Process Development, Process Engineering, etc.) while developing a deep understanding of the manufacturing operations and planning activities within the facility. Responsibilities of the role include: Executing drug product formulation activitiesPerforming initial review of manufacturing batch recordsMaintaining a safe and compliant culture by identifying preventative measuresCreating and/or revising standard operating proceduresLeading continuous improvement initiatives, which may be cross-functional in naturePerforming data analysis (e.g., SPC, CPV) of critical process parameters and making recommendations to Engineering and/or Process Development teamsDeveloping finite schedule for tasks including, but not limited to unit operationsMonitoring productivity and identifying countermeasures for issues impacting cycle time adherenceElevating critical and impactful events to managementPerform the cleaning/sanitization of the manufacturing areas areas and equipment as applicableUtilizing appropriate systems for job duties (SAP, QMTS, and LIMS etc.)Supporting the introduction of new products and technologies into the facilityInitiating and owning quality records, including but not limited to non-conformances (NC), Corrective/Preventative Actions (CAPA) We are all different, yet we all use our unique contributions to serve patients. The Manufacturing professional we seek is a collaborative partner with these qualifications.