QA Manager – Disposition and Quality Systems
Job description
•Mai Cdmo is hiring a QA Manager focused on Disposition and Quality Systems in San Diego, CA. This role is responsible for managing the batch record review and product disposition process, as well as overseeing aspects of the Quality Management System (QMS), including deviations, CAPAs, and change control, ensuring compliance with cGMP regulations. Full job description available upon application via the company careers page.
Preferred experiences
•Significant experience in Quality Assurance within a GMP environment (biotech/pharma), including direct experience with batch record review, product disposition, and managing quality systems. Strong knowledge of FDA/EMA regulations. Leadership or supervisory experience preferred. Bachelor's degree in a scientific field. Full requirements available upon application via the company careers page.
Mai Cdmo
MAI CDMO fosters a collaborative ecosystem within the pharmaceutical industry. We bridge the gap between pharmaceutical companies and CMO/CDMOs, ensuring optimal resource allocation throughout the development process. This collaborative approach empowers our partners to achieve their goals with greater efficiency and focus on what matters most: innovation. Services include CDMO matching, pharmaceutical development consulting, strategic partnership facilitation, and B2B platform management.
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