Krunal Rana, Ms

Krunal Rana, Ms

Car T Quality Assurance Specialist @ Bristol Myers Squibb

About Krunal Rana, Ms

Krunal Rana is a CAR-T Quality Assurance Specialist at Bristol Myers Squibb with extensive experience in quality assurance roles across various pharmaceutical companies.

Title and Current Position

Krunal Rana currently holds the title of CAR-T Quality Assurance Specialist at Bristol Myers Squibb. In this role, he is responsible for the final release of products and maintaining track of batch records. He handles ERP transactions and Corrective and Preventive Actions (CAPA) as part of his quality assurance duties. Additionally, Rana provides critical information to Quality Assurance management to support the decision-making processes within the company.

Previous Experience

Before his current role, Krunal Rana worked at Avet Pharmaceuticals as a Senior Quality Assurance Batch Record Reviewer from 2020 to 2021 for 10 months. Prior to that, he was employed at Aurobindo Pharma USA, Inc. as a QA Batch Record Reviewer from 2019 to 2020 for 11 months in Dayton, New Jersey. From 2018 to 2019, Rana served as a QA Inspector at Vitaquest International LLC for 11 months in New Jersey. Earlier, he was a Senior Quality Assurance Executive at Meril Life Sciences India Pvt Ltd from 2013 to 2017 for 4 years in Vapi. His career began as a QC Chemist at AVIK PHARMACEUTICALS LIMITED, where he worked from 2011 to 2013 for 2 years in Vapi.

Education and Credentials

Krunal Rana obtained his education from two prestigious universities in India. He completed his Master’s degree in Medicinal and Pharmaceutical Chemistry from Sardar Patel University, studying from 2009 to 2011. Prior to that, he earned a Bachelor of Science in Chemistry from Veer Narmad South Gujarat University, Surat, studying from 2006 to 2009. These academic credentials have given him a solid foundation in the field of chemistry and pharmaceutical sciences.

Quality Assurance Expertise

Krunal Rana has extensive experience in reviewing manufacturing and packaging batch records, ensuring compliance with established quality standards. He has been significantly involved in the Annual Product Review (APR) processes to ensure continuous improvement and compliance. His background in batch record review and his ability to handle ERP transactions and CAPA make him a skilled professional in the quality assurance domain.

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