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The Associate Director leads QC analytical testing, ensuring compliance with regulations, managing method validations, and collaborating on regulatory submissions.

Seeking an Associate Director of GMP Quality Assurance to lead QA activities for biologics manufacturing, maintain quality systems, and ensure compliance with regulations. Collaborate with teams to drive improvements and prepare for regulatory inspections.

The Director, Purification Development will manage CDMO processes for drug substance and product production, providing technical leadership and supporting clinical development across teams.

The Associate Director oversees CRAs managing CRO monitoring for clinical trials, ensuring compliance, performance, and process development while leading teams and managing training.