Manpreet Kaur
About Manpreet Kaur
Manpreet Kaur is a System Validation Engineer at BeiGene with over 15 years of experience in the pharmaceutical and biotechnology industries, specializing in computer system validation and quality assurance.
Current Role at BeiGene
Manpreet Kaur is currently employed as a System Validation Engineer at BeiGene. In this role, she is responsible for ensuring that the company's systems are compliant with regulatory standards. Her expertise in system validation helps maintain the integrity and reliability of BeiGene's operational infrastructure.
Previous Experience at Gilead Sciences
From 2016 to 2018, Manpreet Kaur worked at Gilead Sciences as a Validation Engineer/Validation Lead. During her tenure, she led validation projects and managed teams responsible for ensuring the compliance of Gilead’s systems with industry standards and FDA regulations. Her leadership contributed to the successful validation and quality assurance across various projects.
Educational Background in Computer Science
Manpreet Kaur holds a Bachelor of Science (BS) in Computer Science from Doctor Babasaheb Ambedkar Marathwada University. She furthered her studies with a Master of Science (MS) in Computer Science from Illinois Institute of Technology. Her educational background provided a strong foundation for her career in system validation and quality assurance.
Extensive Experience in the Pharmaceutical Industry
Manpreet Kaur has accumulated over 15 years of experience in the pharmaceutical and biotechnology industries. She has worked with several major pharmaceutical companies, including Pfizer, Merck, and Johnson & Johnson. Her roles have ranged from QA Analyst and Validation Consultant to Sr. Quality Assurance Engineer, showcasing her versatility and depth of knowledge in the field.
Expertise in Computer System Validation and Quality Assurance
Specializing in computer system validation and quality assurance, Manpreet Kaur has a proven track record of improving validation processes and ensuring system compliance. She has extensive experience in technical writing and validation consulting, having consulted for leading companies to ensure their systems meet stringent regulatory standards. Her work has been instrumental in ensuring FDA regulation compliance across different projects.