Biologics Cleaning Validation Specialist – On-Site GMP
Listed on 2026-10-12
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Quality Assurance - QA/QC
Quality Engineering -
Manufacturing / Production
Pharmaceutical Manufacturing, Quality Engineering
Amgen in Thousand Oaks seeks a Specialist Manufacturing – Cleaning Validation for the Drug Substance Supply, supporting multi-product biologics manufacturing. You will own validation requirements, lead cross-functional projects from planning to execution, and provide technical support during manufacturing and troubleshooting.
Responsibilities include developing validation strategies and documentation, supporting commissioning and audits, monitoring validation status, and serving as a SME during
We would love to welcome a new Biologics Cleaning Validation Specialist – On-Site GMP to our team in Thousand Oaks, CA, United States.
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This posting is for the Biologics Cleaning Validation Specialist – On-Site GMP role at Amgen, based in Thousand Oaks, CA, United States.
We are looking to fill the Biologics Cleaning Validation Specialist – On-Site GMP position at Amgen in Thousand Oaks, CA, United States.
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