Lead the charge in upstream viral vector manufacturing, driving process development and optimization. Collaborate cross-functionally to enhance production efficiency and ensure robust clinical processes for gene therapy applications.

Join a dynamic team as a Senior Specialist in Quality Control, leveraging your expertise in analytical methods to guide contract laboratories in method development, validation, and troubleshooting, while ensuring compliance and data integrity.

Lead the development and optimization of downstream viral vector purification processes, ensuring robust and scalable production for gene therapy programs. Collaborate cross-functionally to troubleshoot and enhance manufacturing operations.

Contribute to regulatory compliance by reviewing promotional materials, guiding marketing strategy, and ensuring alignment with FDA guidelines. You'll collaborate across teams to promote effective strategies while navigating complex regulatory landscapes.

Join a dedicated team in delivering pivotal insights for clinical trials. Utilize SAS to manage datasets, ensure regulatory compliance, and support comprehensive submissions for both investigational and marketed products.