Senior CQV Manager - GMP Validation & Sterilization
Listed on 2026-10-07
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Pharmaceutical
Validation Engineer, Pharmaceutical Manufacturing, Pharma Engineer
Siegfried in Irvine, CA seeks a senior CQV leader to oversee commissioning, qualification and validation for drug products, devices, and manufacturing processes. You will own the site validation strategy and manage master plans, protocols and reports, coordinating cross-functional teams and external consultants.
Ideal candidates have 6–10 years in FDA/GMP environments, aseptic manufacturing experience, and strong leadership.
Consider building your career as a Senior CQV Manager - GMP Validation & Sterilization at Siegfried.
The Senior CQV Manager - GMP Validation & Sterilization position in the IT & Technology, Engineering field is open for applications.
We have an opening for a Senior CQV Manager - GMP Validation & Sterilization in Irvine, CA, United States within IT & Technology, Engineering.
This role, Senior CQV Manager - GMP Validation & Sterilization at Siegfried, could be your next opportunity.
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