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Specialist Manufacturing - Drug Product; DP Operations

Job in Thousand Oaks, Ventura County, California, 91362, USA
Listing for: Amgen SA
Full Time position
Listed on 2025-12-18
Job specializations:
  • Engineering
    Process Engineer, Manufacturing Engineer
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below
Position: Specialist Manufacturing - Drug Product (DP) Operations

Join Amgen’s Mission of Serving Patients

At 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. 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.

Specialist Manufacturing - Drug Product Operations

What you will do

Let’s do this. Let’s change the world. At Amgen, our mission—to serve patients—drives everything we do. As a Specialist Manufacturing in Drug Product (DP) Operations within the Production Process Owner (PPO) Team at our Thousand 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-functional teams—including Engineering, Quality, Process Development, and Operations—to implement process improvements, support new technology introductions, and maintain robust GMP manufacturing performance. Your work will directly contribute to Amgen’s ability to deliver life-changing therapies to patients worldwide.

Key Responsibilities:

Documentation and Process Management

  • Initiate, revise, and approve controlled manufacturing documents within Amgen’s 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 accurately reflect operational practices and regulatory requirements.

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.

  • Assist in developing and implementing SOPs, batch records, training, validation, and automation configurations.

Operational Performance and Data Analytics

  • Analyze manufacturing data and performance metrics to identify trends, deviations, and opportunities for improvement.

  • Develop and implement data-driven solutions to improve yield, reliability, and compliance.

  • Support data monitoring using analytical tools such as Enterprise Data Lake and Spotfire, ensuring configuration alignment with process design and GMP requirements.

Deviation and CAPA Management

  • Support timely investigation 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

  • Assist in developing and implementing process validation protocols and reports.

  • Collect, analyze, and interpret validation and process monitoring data to ensure process robustness and compliance.

  • Support establishment of process parameters, control limits, and performance reporting.

Change Control and Continuous Improvement

  • Support change control activities to ensure GMP, regulatory, and operational compliance.

  • Evaluate and justify process or equipment changes and assist with project execution.

  • Participate in continuous improvement and operational excellence initiatives to enhance safety, quality, and efficiency within DP operations.

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is an individual with these qualifications.

Basic Qualifications:

  • Doctorate…

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