Frederick has been performing various types of equipment and process validation projects for over 30 years in the medical device, pharmaceutical, and biologics industries.
Frederick Wiles uses his extensive knowledge in regulatory compliance (cGMP and QSR) and industry standards to help clients with their highly technical projects and initiatives. He began his career as a metrologist developing measurement standards for analytical method and environmental monitoring instrumentation. Soon after, Frederick’s career path shifted to validation and quality engineering.
As a quality engineer, Frederick has contributed his strong statistical and mathematical background to helping clients with complex projects such as characterization and validation of both discrete and batch manufacturing processes, statistical analysis of critical-to-quality product data, and implementation of statistical process control methods and techniques.
Frederick has written numerous articles on the application of statistics for measurement systems and process validation.
He is a Principal Validation Consultant, working on and managing equipment and process validation projects for our customers. He holds an ASQ certification in quality engineering (CQE).
Contact Frederick about Equipment and Process Validation
Our Trainers are Certified by PMI, Six Sigma, and The American Society for Quality Training
