Job Duties:
1.Formulation preparation for in-house studies

• Planning and conducting formulation research and development activities for preclinical studies.
• Preparation of oral and parenteral dosing formulations of test compounds for non-clinical early and later-stage toxicology studies.
• Compile method templates/ batch formulation records/ancillary documents.
• Handle pharmaceutical materials, excipients, oral dosage forms and parenterals.
• Coordinate formulation preparation activities with CRO partners, as needed.

2. Support and manage logistics of test item and vehicle/diluent

• Organize and facilitate logistics of requests (internal transfers and out-going shipments)
• Plan and prioritize per project timeline needs for domestic and international shipments
• Execution of requests (out-going shipments or internal transfers). Organize and transfer physical materials per requests from internal laboratories. Prepare material to be shipped to CROs, assemble packaging supplies, and provide temperature monitor to ensure material experience recommended storage conditions during shipment duration.   
• Documentation/Coordination of request: Coordinate shipments, communicate with International (Imports Compliance) and supporting functions, logistics dock, send tracking number to CRO
• Inventory management- Receive and store physical materials (test item and vehicle /diluent) per SOPs. Manage inventory lifecycle as per SOP

3. Prepare records for archival as per SOPs and GLP requirements.

4. Lab duties- Ensuring EHS compliance, and conduction of regular lab inspection.  Organization of supplies in the laboratory and in storage area.

•  Excellent organization and communication skills
• Know how to use MS Office (Excel, Word, PowerPoint, MS Teams)
• Ability to multitask
• Proactive attitude
• Knowledge of database use a plus
• Familiarity with a quality environment (GLP) a plus

Education Requirements:

•    BA/BS