Jacek Cieslak utilizes a methodical approach, scrutinizing risk management processes and controls, procedural adherence, and facility maintenance. He places a strong emphasis on thorough investigations, root cause analysis, and compliance with regulatory standards to ensure the quality, safety, and integrity of the manufacturing processes and facility.

Jacek Cieslak is a detail-oriented FDA auditor who focuses on assessing the risk management and control of manufacturing processes, material management systems, cleaning and sanitization procedures, root cause analysis, microbial control, procedural controls for electronic data, and facility and equipment design, maintenance, and labeling. He looks for thorough risk assessments, comprehensive monitoring and control of processes, adherence to procedures, effective root cause analysis and CAPA implementation, robust microbial control, and proper design, maintenance, and labeling of facilities and equipment.