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Amgen Logo Amgen · Manufacturing

Associate Manufacturing

United States, Thousand Oaks 70985.20 - 96038.80 USD / Year · Job Posted July 03, 2026
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Job Description

The Associate of Manufacturing will work in a dynamic production environment at the Amgen Thousand Oaks Drug Substance plant, supporting development, clinical, and launch activities. Under general supervision, this role performs manufacturing operations within Building 23 in accordance with Standard Operating Procedures (SOPs). This position is responsible for hands-on manufacturing operations, including setup, cleaning, sanitization, media and buffer preparation, and analytical testing.

Job Responsibility

  • Perform and monitor critical manufacturing processes
  • Execute routine validation protocols
  • Comply with GMP requirements and all safety and compliance expectations
  • Draft and revise routine documents such as MPs, SOPs, and technical reports
  • Initiate and own quality records, including CAPA and CAPA-EV
  • Identify and recommend improvements to routine functions and implement approved changes
  • Perform basic troubleshooting and accurately recognize and report problems
  • Direct operators on critical processes
  • Assist in the review of documentation for assigned functions, including routine area audits and batch records
  • Perform activities that may include rigorous and repetitive work
  • Work around high-pressure systems and occasionally around heavy equipment
  • Train staff on hands-on tasks, as needed
  • Serve as a safety representative, as needed
  • Participate on cross-functional teams and represent Manufacturing, as needed
  • Apply technical, scientific, operational, and compliance knowledge to support implementation of new technologies into the plant
  • Demonstrate strategic problem-solving skills and champion continuous improvement

Requirements

  • High school diploma / GED and 2 years of manufacturing or operations work experience
  • Associate degree and 6 months of manufacturing or operations work experience
  • Bachelor's degree

Nice to have

  • Bachelor's degree in science or engineering
  • Knowledge of large-scale biotechnology operations such as purification, cell culture, and aseptic processing
  • Knowledge of single-use systems
  • CFR and regulatory knowledge
  • Mechanical aptitude
  • Basic statistical and mathematical skills
  • Ability to interpret and apply GMP knowledge
  • Understanding of analytical methods used in a manufacturing environment
  • Demonstrated technical writing capability
  • Project management and presentation skills
  • Ability to understand, apply, and evaluate basic chemistry, biology, and physical principles
  • Basic troubleshooting skills for production equipment
  • Experience with Delta V
  • Experience with lab equipment and testing

What we offer

  • Retirement and Savings Plan with generous company contributions
  • Group medical, dental and vision coverage
  • Life and disability insurance
  • Flexible spending accounts
  • Discretionary annual bonus program
  • Stock-based long-term incentives
  • Award-winning time-off plans
  • Flexible work models where possible
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