Carroll Davis

A senior QC Lab analyst with over 14 years working knowledge of cGMP regulations in QC lab operations. Responsible for maintaining a compliant and efficient QC lab that analyzed in process, raw material, intermediate and final release samples. This included lab set-up and design; equipment life cycle; assay transfers; training and mentoring co-workers; change control, exception reports, CAPA with root cause analysis; GMP documentation and working knowledge of quality systems. Recognized for timely laboratory testing, data analysis, review and reporting following written procedures while meeting and exceeding turn around goals in an in-process cGMP manufacturing support lab. The ability to multi-task, understand clients needs, be open-minded and flexible while being well organized and having strong attention to details enable me to thrive in an regulated environment where meeting strict deadlines with constantly changing priorities is often recognized.