Purpose: 

• Responsible for adhering to Cleaning Validation Master Plans and strategies for initial and periodic re-validation.
• Responsible for ensuring risk based cleaning validation policies and standards have robust quality oversight and are in compliance to GMP standards and AbbVie policies and procedures.

Major Responsibilities:

• Adhere to appropriate validation master plans, validation execution plans, and procedures related to risk based cleaning validation of equipment and processes in the AbbVie Operations Campus in Tuas, Singapore comprising of both API and Biologics manufacturing facilities.
• Generate, execute, and review protocols for initial and subsequent re-qualification programs related to cleaning verification / validation to ensure equipment and cleaning processes are maintained in a validated state.
• Support the development of specifications and str...