Namisha Bansal

Namisha Bansal

Sr Manager Qa @ BeiGene

About Namisha Bansal

Namisha Bansal is a Senior Manager of QA at BeiGene in California, specializing in regulatory compliance and quality assurance within the pharmaceutical and biotech industries.

Company

Namisha Bansal is currently employed at BeiGene in California, United States. She holds the position of Senior Manager in Quality Assurance (QA). Additionally, she holds the role of Manager Clinical System Validation at BeiGene in the San Francisco Bay Area. She also works at Gilead Sciences as a Validation Lead for Oracle ERP and Oracle Middleware. Her career includes past roles at Abbott and Global Pharma.

Title

Namisha Bansal serves as a Senior Manager in Quality Assurance (QA) at BeiGene. She also manages clinical system validation in the San Francisco Bay Area for the same company. At Gilead Sciences, she holds the position of Validation Lead for Oracle ERP and Oracle Middleware.

Education and Expertise

Namisha Bansal earned her Bachelor's Degree in Electrical and Electronics Engineering from Kurukshetra University, where she studied from 2000 to 2004. She has significant expertise in managing and validating various systems, including MES, LIMS, CTMS, IRT, and multiple Veeva platforms. Her specialty areas include regulatory compliance, quality assurance, GAMP, 21 CFR Part 11, and risk management.

Background

Namisha Bansal has a strong background in validation and qualification processes within the pharmaceutical and biotech industries. She has worked at multiple renowned organizations, including Abbott and Global Pharma, where she honed her skills in validation and compliance. At Abbott, she served as Validation Lead and Senior Validation Consultant, while at Global Pharma, she worked as a Validation Engineer.

Achievements

Throughout her career, Namisha Bansal has amassed extensive experience in vendor audits and regulatory inspections. She is skilled in change management and CAPA (Corrective and Preventive Actions). Her role has covered a broad spectrum of validation activities in the pharmaceutical and biotech industries, strengthening her background in ensuring regulatory compliance and quality assurance.

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