Manufacturing Contractor I

Perform routine clinical manufacturing operations in a cGMP-regulated environment, including weighing and dispensing, solution preparation, and equipment CIP/COP. Maintain a safe and compliant manufacturing environment. Interact with cross-functional support groups to ensure timely and accurate completion of activities.

Requirements

• Perform routine clinical manufacturing operations in a cGMP-regulated environment
• Operate production equipment according to approved SOPs for clinical product manufacturing
• Accurately document all manufacturing activities using existing forms and records
• Maintain a safe, clean, and compliant manufacturing environment at all times
• Interact with cross-functional support groups such as Facilities, Quality Control (QC), Quality Assurance (QA), Materials Management, and EHS to ensure timely and accurate completion of activities