GMP Quality Assurance Lead – Associate Director
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Quality Assurance - QA/QC
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Healthcare
Job Description & How to Apply Below
Travere Therapeutics in San Diego, with remote flexibility, is seeking an Associate Director of Quality Assurance - Technical to provide technical quality guidance across contract manufacturing, testing, storage, and distribution.
You will lead GMP QA functions, oversee CSPs through Phase 3, manage validation efforts, and drive CAPA, change control, and risk management while ensuring compliance with CFR/ICH and regulatory standards.
Are you ready to take on the GMP Quality Assurance Lead – Associate Director role at Travere Therapeutics?
As a GMP Quality Assurance Lead – Associate Director, you will play an important part at Travere Therapeutics in Wichita, KS, United States.
We invite applications for the GMP Quality Assurance Lead – Associate Director position located in Wichita, KS, United States.
The following position is for a GMP Quality Assurance Lead – Associate Director with Travere Therapeutics.
Position Requirements
10+ Years work experience(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
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