Seeking an experienced Biopharmaceutical Data Scientist to develop statistical strategies, analyze manufacturing processes, and create reproducible data products. Collaboration with scientists and adherence to GMP standards are essential.

The Associate Scientist will support the Lentiviral Vector Drug Product team through stability studies, particle analysis, and laboratory management, fostering collaboration across functions.

The Senior Director of Biometrics will lead the Biometrics function in clinical development, providing strategic and scientific leadership, managing teams, and ensuring compliance with regulatory standards.

The Bioprocessing Specialist will manage downstream manufacturing operations, lead purification initiatives, and ensure compliance with GMP standards in a clean-room environment.

The role involves supporting downstream manufacturing operations including buffer preparation, chromatography, and material management in a GMP facility, ensuring compliance and quality of gene therapy products.

The Senior Analyst, Quality Control Analytical will perform QC testing, support method development, and lead improvement initiatives within the QC analytical team.