Responsible for Chemotherapy Compounding and Reconciliation in accordance with USP Chapter <797-800> Compliance and Documentation.
Works with the quality coordinator to ensure that policies and procedures are current and that all compounding activities are in compliance with USP and MOH regulations.
Coordinates regular sterility and stability testing of the stock sterile products in compliance with USP and MOH regulations.
Oversees all documentation related to sterile product production.
Management of end product process prior to distribution.
Ensures all compounding and testing records are accurate and complete.
Accurately prepares and labels sterile products in a safe and cost-effective manner, utilizing an aseptic technique.
Maintains adequate stock of supplies necessary for compounding and cleaning of the Sterile Compounding Area. <...