Associate Manufacturing - Thousand Oaks CA

Associate ManufacturingAt Amgen, if you feel like you're part of something bigger, it's because you are. Our shared missionto serve patients living with serious illnessesdrives all that we do. Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas Oncology, Inflammation, General Medicine, and Rare Disease we reach millions of patients each year. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.What You Will Do:Let'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 filling 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 managementApplying 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)