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Lead downstream process development for viral vector production, ensuring optimized processes, compliance with cGMP regulations, and collaboration across teams while maintaining quality and safety standards.

The Quality Assurance Specialist II ensures compliance in gene therapy manufacturing operations, overseeing quality management systems and supporting internal audits. Responsibilities include batch record reviews, investigations, and collaboration with manufacturing teams.

The Supply Chain Analyst – Buyer/Planner will handle demand planning, procurement, and vendor management, ensuring timely delivery and cost efficiency in operations.

The QC Analyst will perform routine and non-routine QC testing and sampling, ensuring compliance with cGMP standards while supporting quality systems and monitoring. This role includes environmental testing and maintaining QC microbiology systems.