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Senior Manager Manufacturing – Production Process Owners

at Amgen

AmgenUS - California - Thousand OaksPosted 2026-06-05
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Job description

Career CategoryManufacturingJob DescriptionJoin Amgen’s Mission of Serving PatientsAt Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives 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. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. 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.Senior Manager, Manufacturing Programs – Production Process OwnersWhat you will doLet’s do this. Let’s change the world!In this vital role you will be a people leader and cross-functional integrator responsible for end-to-end process governance and execution support within Drug Product Supply operations at the Thousand Oaks campus.This role ensures the site maintains a strong operating system for manufacturing readiness, technical governance, issue resolution, and continuous improvement across multiple unit operations and enabling processes, with accountability for driving alignment across key site forums, priorities, and decision-making bodies.Key Responsibilities:Leadership & Team ManagementLead, coach, mentor, and develop the manufacturing process owners within the manufacturing organization.Foster a culture of collaboration, continuous improvement, accountability, and high performance across the team.Provide guidance, performance feedback, and support for career development plans for direct reports.Set clear priorities, define role clarity, and establish coverage plans so the PPO team can flex across site needs, emerging issues, and evolving operational demands.Manufacturing Operations ManagementEnsure strong collaboration and coordination between Manufacturing and key partners such as Quality, Facilities and Engineering, Automation, Supply Chain, Maintenance, and other site functions.Provide governance and execution support to ensure smooth, compliant, and reliable manufacturing operations.Manage and improve manufacturing processes to increase productivity, reduce waste, and maintain product quality and compliance.Strengthen process discipline, documentation quality, and operational readiness across site processes.Serve as an escalation point for complex execution topics, ensuring issues are evaluated, decisions are made with the right stakeholders, and actions are closed with discipline.Quality, Compliance & Regulatory OversightEnsure manufacturing activities are performed in compliance with cGMP and all applicable regulatory requirements and internal quality standards.Support inspection and audit readiness by ensuring appropriate documentation, escalation pathways, and governance transparency.Support site teams that own compliance-critical programs, including aseptic compliance and validation-related execution, by helping prioritize resources and drive timely resolution of issues.Ensure disciplined execution and timely closure of quality actions, CAPAs, and effectiveness verification activities in partnership with Quality and subject matter experts.Support and reinforce a strong safety culture and a safe working environment for all employees.Process Optimization & Continuous ImprovementProvide oversight and drive process improvement initiatives aimed at increasing efficiency, improving reliability, reducing costs, and enhancing the drug product manufacturing process.Use lean manufacturing and other continuous improvement tools to identify opportunities and optimize operations.Analyze operational and quality data to identify trends, solve complex problems, and implement corrective actions.Collaboration & Cross-Functional CommunicationPartner with site stakeholders to ensure readiness for new processes, new products, and major operational changes.Support risk identification, issue resolution, and execution readiness across impacted functions and unit operations.Facilitate, or ensure strong facilitation of, key site governance forums used to align priorities, remove barriers, and drive execution.Support the site project governance operating model, including plant project prioritization, by driving disciplined intake, prioritization, execution tracking, and escalation when needed.Act as a point of contact for process owners during troubleshooting and resolution of manufacturing-related issues.Technology IntegrationStay current on technological advancements and assess opportunities for adoption in the plant.Support introduction and scale-up of new technologies, equipment, and systems that enhance production capabilities and improve operational performance.Partner cross-functionally to ensure technology-related changes are effectively planned, implemented, and sustainedWhat we expect of youWe 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.Basic Qualifications: Doctorate degree and 2 years of Manufacturing and Operations experience ORMaster’s degree and 6 years of Manufacturing and Operations experience ORBachelor’s degree and 8 years of Manufacturing and Operations experience ORAssociate’s degree and 10 years of Manufacturing and Operations experience ORHigh school diploma / GED and 12 years of  Manufacturing and Operations experienceIn a
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