Join Amgenâs Mission of Serving Patients
At Amgen, if you feel like youâre part of something bigger, itâs because you are. Our shared missionâto serve patients living with serious illnessesâdrives all that we do.
Since 1980, weâve helped pioneer the world of biotech in our fight against the worldâs toughest diseases. With our focus on four therapeutic areas âOncology, Inflammation, General Medicine, and Rare Diseaseâ 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, youâll 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, youâll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
Specialist Manufacturing - DP Production Process Owner
What you will do
Letâs do this. Letâs change the world. At Amgen, our missionâto serve patientsâdrives everything we do. As aSpecialist Manufacturing in Drug Product (DP) Operations as a Production Process Ownerat ourThousand Oaks (ATO)manufacturing site, you will play a key role in ensuring our commercial and clinical manufacturing processes are compliant, efficient, and continuously improving.
You will partner with cross-functionalteamsâincluding Engineering, Quality, Process Development, and Operationsâto implement process improvements, supportnew technologyintroductions, andmaintainrobust GMP manufacturing performance. Your work will directly contribute to Amgenâs ability to deliver life-changing therapies to patients worldwide.
Key Responsibilities
Change Control and Continuous Improvement
Support change control activities to ensure GMP, regulatory, and operational compliance.
Evaluate and justify process or equipment changes andassistwith project execution.
Participate in continuous improvement and operational excellence initiatives to enhance safety, quality, and efficiency within DP operations.
Process Implementation and Project Execution
Support implementation of new processes, equipment, and major initiatives within Drug Product operations.
Collaborate with Capital, Engineering, Process Development, Quality, and other functions to define requirements and achieve operational readiness.
Assistin developing and implementing SOPs, batch records, training, validation, and automation configurations.
Operational Performance and Data Analytics
Analyze manufacturing data and performance metrics toidentifytrends, deviations, and opportunities for improvement.
Develop and implement data-driven solutions to improve yield, reliability, and compliance.
Support data monitoring using analytical tools such asâŻEnterprise Data LakeandâŻSpotfire, ensuring configuration alignment with process design and GMP requirements.
Deviation and CAPA Management
Supporttimelyinvestigation and resolution of manufacturing deviations.
Participate in root cause analyses (RCA) and human performance evaluations.
Contribute to the development and implementation of effective corrective and preventive actions (CAPAs) and monitor CAPA effectiveness.
Validation and Process Control
Assistin developing and executing process validation protocols and reports.
Collect, analyze, and interpret validation and process monitoring data to ensure process robustness and compliance.
Supportestablishmentof process parameters, control limits, and performance reporting.
Documentation and Process Management
Initiate, revise, and approve controlled manufacturing documents within Amgenâs electronic document management system (CDOCs).
Serve as document author, owner, reviewer, or data verifier, ensuring accuracy and compliance with current GMP and Amgen standards.
Maintain documentation to accuratelyreflectoperational practices and regulatory requirements.
Basic Qualifications
Doctorate degreeOR
Masterâs degree and 2 years of Manufacturing support experienceOR
Bachelorâs degree and 4 years of Manufacturing support experience OR
Associateâs degree and 8 years of Manufacturing support experienceOR
High school diploma / GED and 10 years of Manufacturing support experience
Preferred Qualifications
Advanced degree (Masterâsor Ph.D.) in Engineering, Biotechnology, or related field
Experience in aseptic Drug Product or biologics manufacturing
Knowledge of process validation, deviation management, and change control
Strong analytical and problem-solving skills with experience using data visualization tools (Spotfire, JMP, Excel)
Excellent written and verbal communication skills and ability to collaborate across functions
Competencies for Success
Operational Excellence:Demonstratesattention to detail, prioritizes quality and compliance, and drives process improvements.
Technical Expertise:Applies technical knowledge to evaluate, troubleshoot, andoptimizemanufacturing processes.
Collaboration:Builds strong cross-functional relationships and fosters teamwork across disciplines.
Accountability:Takes ownership of deliverables and ensurestimelycompletion of commitments.
Continuous Improvement:Identifiesand implements opportunities to enhance manufacturing performance and reliability.
What you can expect from us
As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, weâll support your journey every step of the wa
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