Quality Assurance Validation Specialist - GMP & CSV
Listed on 2026-10-07
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Quality Assurance - QA/QC
QA Specialist - Analyst/Manager, Quality Control - QC Analysts/Managers, Regulatory Compliance Specialist, Quality Engineering -
Pharmaceutical
Regulatory Compliance Specialist, Quality Engineering
Takeda Pharmaceutical Co. in Thousand Oaks, CA, is seeking a Quality Assurance Validation Associate to provide QA oversight of validation deliverables and change controls across facilities, utilities, equipment, and computer systems validation.
You will review Master Plans and IQ/OQ/PQ/CSV packages, assess risk, ensure traceability, and support regulatory submissions. The role requires GMP experience, data integrity focus, and collaboration with cross-functional teams.
Step into the Quality Assurance Validation Specialist - GMP & CSV role at Takeda Pharmaceutical Co. in Thousand Oaks, CA, United States and grow with us.
This opportunity is for the Quality Assurance Validation Specialist - GMP & CSV role at Takeda Pharmaceutical Co.
We are seeking a motivated Quality Assurance Validation Specialist - GMP & CSV to join Takeda Pharmaceutical Co. in Thousand Oaks, CA, United States.
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