The Logistics Coordinator supports Lab Operations by managing external sample logistics, coordinating with project leads, and maintaining sample inventory and registration.

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.

The Technical Development Scientist will design experiments for gene therapy product development, optimize processes, analyze data, and collaborate cross-functionally to ensure compliance and quality.

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.

Manage end-to-end clinical cold-chain logistics for cGMP materials—design shipping lanes, oversee couriers, customs, temperature control, inventory, excursion investigations, SOPs, vendor performance, and ensure regulatory compliance for international shipments.

Provide QA leadership and independent oversight of QC activities for drug substance/product and release testing. Ensure cGMP compliance, data integrity, method lifecycle management, investigations, change control, CAPAs, and inspection readiness while partnering with QC and cross-functional teams.

Lead design, validation, and lifecycle management of IRT systems for clinical trials. Translate protocol into IRT specifications, govern change control, manage vendor relationships, lead UAT/validation, monitor live performance, troubleshoot shipments and inventory, ensure regulatory inspection readiness, and align cross-functional teams on supply strategy and IRT operations.

The QA Project Manager leads quality assurance efforts for clinical projects, ensuring compliance with regulations and effective cross-functional collaboration.

The Quality Control Analyst will conduct release testing for clinical products, analyze data, guide junior staff, and engage in method validation and troubleshooting.

The QC Project Manager will manage Quality Control project timelines, coordinate cross-functional activities, identify risks, facilitate meetings, and ensure effective communication among stakeholders in a GMP environment.