Shift    1st (8am-5pm)
Hours    8am-5pm

Ensure the safe, timely, and fully compliant shipment of research, development, and clinical trial materials to domestic and international sites and study locations.

Ensure the safe, timely, and fully compliant shipment of research, development, and clinical trial materials to domestic and international sites and study locations. Manage end‑to‑end logistics, maintain strict adherence to U.S. Department of Transportation (DOT) and International Air Transport Association (IATA) regulations, and support technical operations by coordinating the movement of regulated materials with accuracy, documentation integrity, and exceptional attention to detail.  Monitor and maintain chain of custody documentation during receipt, shipment, transfer, return, & disposal. Ensure appropriate product storage conditions are maintained throughout the material transfer process. Ensure proper records maintenance (e.g. COA/COC, MSDS, NOS, label approval, shipment manifest) per relevant SOP's, internal policies & study protocols. Comply with applicable regulations including but not limited to FDA, CVM, CFR, USDOT, USDA, IATA & USFAA. 

May lead special projects, internal audits and non-routine activities, as needed or requested.  Possesses the ability to set up and execute shipments from start to finish and coordinate with the appropriate personnel to ensure timelines are met.

The output of this role is governed by regulatory GXP requirements, US and international shipping regulations, and BI quality standards globally. 

Physical Demands / Surroundings:  
o Lifting, carrying, pushing and pulling –