Top Tech Jobs & Startup Jobs

The Principal Scientist will optimize AAV downstream processes, lead purification development, support regulatory compliance, and collaborate across functions for gene therapy programs.

The QA Specialist I will organize and manage document control activities, ensuring proper filing, adherence to standards, and document integrity. Responsibilities include organizing QA documents, conducting reconciliations, and supporting inspections while maintaining safety protocols.

The QC Analyst will perform release testing, analyze data, develop SOPs, conduct qualitative studies, and guide junior staff in a biotech setting.

Support design and execution of clinical development activities for ophthalmology trials: protocol writing, vendor/CRO oversight, medical monitoring, data review/interpretation, regulatory document contributions, and cross-functional collaboration.

The QA Manager, Document Control will oversee Document Control and quality system maintenance, system administration of MasterControl EQMS, training, and managing controlled documents.

The Clinical Data Manager oversees data management activities across clinical studies, ensuring data compliance and quality from start-up to closure, while managing CRO vendors and leading the data management team.

Lead quality assurance activities for cell and viral banks and drug products, ensuring compliance with cGMP and regulatory requirements, and collaborate cross-functionally for lot disposition.