Linh Truong
About Linh Truong
Linh Truong is a Quality Investigator with expertise in risk assessment and root cause analysis, currently working at QuVa Pharma, Inc. in Sugar Land, Texas. With a background in quality assurance and extensive experience in compliance and auditing, Truong holds certifications in pharmaceutical quality and has a Master of Business Administration from the University of Houston-Victoria.
Current Role at QuVa Pharma
Linh Truong currently serves as a Quality Investigator at QuVa Pharma, Inc., a position held since 2020. Based in Sugar Land, Texas, Truong is responsible for identifying and mitigating potential quality issues through risk assessment and root cause analysis. This role involves extensive experience in conducting internal and FDA audits, ensuring compliance with relevant regulations, and leading corrective and preventive actions to enhance quality systems.
Previous Experience in Quality Assurance
Prior to the current role, Linh Truong worked at QuVa Pharma, Inc. as a Quality Assurance Specialist from 2016 to 2017. Additionally, Truong served as a Quality Assurance Investigator at PharMEDium Services from 2018 to 2020, where responsibilities included managing out-of-specification investigations and ensuring compliance with Good Manufacturing Practices (GMP). Truong also gained experience as a QA Auditor and Quality Control Specialist at Eagle Analytical from 2013 to 2018.
Education and Certifications
Linh Truong holds a Master of Business Administration (MBA) from the University of Houston-Victoria, completed between 2019 and 2021. Truong is certified as a Certified Pharmaceutical cGMP Professional (ASQ-CPGP) and a Certified Quality Auditor (ASQ-CQA). These qualifications support Truong's expertise in Good Documentation Practices (GDP) and Standard Operating Procedures (SOPs) within GMP environments.
Expertise in Quality Management
Truong possesses extensive expertise in risk assessment, root cause analysis, and environmental monitoring within clean room environments. Proficient in process validation and cleaning validation, Truong ensures compliance and quality in pharmaceutical manufacturing. The focus on managing quality events, deviations, and customer complaints further highlights Truong's commitment to maintaining high standards in quality management.
Specialization in Auditing and Compliance
Linh Truong specializes in conducting internal and FDA audits, with a focus on compliance with 21CFR part 11 and part 210 regulations. This specialization includes leading corrective actions and preventive actions (CAPA) to continuously improve quality systems. Truong's background in quality assurance and control positions them as a knowledgeable professional in the pharmaceutical industry.