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The Analytical Development Manager leads analytical method development, validation, and tech transfer in a cGMP environment while managing teams, ensuring quality and communication with clients.

The Senior Associate, Quality Assurance ensures compliance with GMP in cell and gene therapy manufacturing by managing quality systems, documentation, and cross-functional collaboration.

The Associate II, Quality Assurance will support quality operation activities, ensuring compliance with cGMPs, authoring SOPs, and overseeing document management.

The QC Analyst III will lead quality control activities including raw material testing and environmental monitoring, ensuring compliance with GMP practices.