Onsite QA Associate, Drug Substance; GMP
Job in
Thousand Oaks, Ventura County, California, 91362, USA
Listing for:
Aditi Consulting
Full Time, Contract
position
Listed on 2026-11-14
Job specializations:
-
Quality Assurance - QA/QC
-
Healthcare
Job Description & How to Apply Below
A leading consulting firm in California is seeking a Senior Associate, Quality Assurance to oversee Drug Substance manufacturing areas and ensure compliance within a GMP environment. The role involves real-time QA support, along with responsibilities like batch record review and SOP approvals. Ideal candidates will have a Bachelor’s Degree in a relevant field, hands-on QA or manufacturing experience, and strong critical thinking skills.
Full-time employees receive comprehensive benefits including health insurance and retirement plans.
As a Contract Onsite QA Associate, Drug Substance (GMP), you will play an important part at Aditi Consulting in Thousand Oaks, CA, United States. The following opening is for a Contract Onsite QA Associate, Drug Substance (GMP) with Aditi Consulting. Our group is growing, and we are hiring a Contract Onsite QA Associate, Drug Substance (GMP) in Thousand Oaks, CA, United States.
Position Requirements
10+ Years work experienceTo View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
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