Lee
molecular biology
Farmacore Biotechnology
Swaziland
Biography
Lucy has nearly 25 years of experience in GLP and GMP regulated contract pharmaceutical laboratories. Lucy is responsible for providing leadership in development and implementation of an independent quality system to support lab operations for CMIC, Inc.; for identifying areas of regulatory risk and bringing these to the attention of lab and senior management; for developing and executing training for all CMIC, Inc. employees on quality assurance policies, programs, initiatives and GLP regulatory requirements; for writing, reviewing, and approving (where applicable) procedures and quality documentation. She is also leading an effective Quality Assurance Team to ensure lab operations are in compliance with GLP requirements.
Research Interest
Lucy has nearly 25 years of experience in GLP and GMP regulated contract pharmaceutical laboratories. Lucy is responsible for providing leadership in development and implementation of an independent quality system to support lab operations for CMIC, Inc.; for identifying areas of regulatory risk and bringing these to the attention of lab and senior management; for developing and executing training for all CMIC, Inc. employees on quality assurance policies, programs, initiatives and GLP regulatory requirements; for writing, reviewing, and approving (where applicable) procedures and quality documentation. She is also leading an effective Quality Assurance Team to ensure lab operations are in compliance with GLP requirements.
