About this opportunity
Aditi Consulting lists this Contract Onsite QA Associate, Drug Substance (GMP) opportunity in thousand oaks, California. Review the employer’s description below for duties, qualifications and application requirements.
Job description
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.
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Worksite address
thousand oaks, CA, 91362, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.