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The Lead QC Associate oversees QC analysts, executes tests for gene therapy products, ensures compliance with GMP, and maintains lab records.

The Sr. Associate will manage product disposition activities, batch record reviews, quality assurance support, and ensure compliance with cGMP standards.

The Strategic Operations Intern will support business operations and marketing initiatives, assist with financial reporting, and drive process efficiency, while collaborating on cross-functional projects.

The intern will support internal communications and employee experience initiatives, creating various content types and collaborating on engagement strategies while gaining exposure to corporate affairs functions.

The Associate Director of Market Access and Reimbursement serves as a contact to assist healthcare providers with access and reimbursement issues for Sarepta's therapies, ensuring site readiness and engagement to facilitate patient access.

The QC Associate II will conduct gene therapy product testing using cell-based and ELISA methods while ensuring compliance with cGMP regulations. Responsibilities include sample preparation, troubleshooting, data analysis, and maintaining lab compliance documentation.

The QC Associate II will conduct testing of gene therapy products, ensure compliance with cGMP, and assist in quality event management.