Developed standardized documentation to ensure regulatory compliance.
Resulted in a 20% increase in user satisfaction and a 30% improvement in documentation adherence across teams.
Enhanced operational efficiency by implementing quality management processes and piloting the Microsoft Power Apps Document Request Form for better user support.
Led training sessions on GDP and GMP quality management practices, closing knowledge gaps among employees, and increasing GDP competency.
Supported batch release and approval of internal certificate reports for samples in gLIMS, ensuring timely compliance with regulatory requirements.
LEAD DEVIATIONS INVESTIGATOR
Almac Clinical Services
Durham, North Carolina
01.2022 - 10.2022
Established comprehensive framework for documenting and trending deviation data, enhancing cross-functional collaboration.
Conducted targeted training sessions on investigation protocols, resulting in improved team proficiency.
Achieved 30% increase in compliance through enhanced clarity in complex reports.
Reduced investigation cycle time by 25% through optimized reporting processes.
Identified gaps in understanding of deviation reporting, initiating focused training initiatives.
Improved quality of investigations and accuracy of data tracking across teams.
Boosted team confidence in reporting and resolution protocols through effective training.
TECHNICAL WRITER II
Merck
Durham, NC
07.2019 - 07.2021
Created user manuals and conducted usability testing to enhance documentation quality.
Achieved 20% reduction in support calls regarding user manuals, indicating improved clarity.
Addressed user struggles with software functionalities by developing comprehensive documentation.