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The Lead Specialist, QA - Batch Disposition is responsible for providing Quality Assurance support for GMP documentation related to master/working cell banks, bulk drug substance, and finished drug products in a state-of-the-art CGMP manufacturing facility for Gene Therapies. This role involves reviewing documentation, ensuring compliance with regulatory standards, and identifying areas for quality improvement. The position requires continuous monitoring of systems and procedures to maintain compliance and support the development and manufacturing of advanced therapeutic products.