Executive/Senior Executive

As an Executive/Senior Executive in the R&D Quality-CMC QA department at Sun Pharmaceutical Industries Limited in Gurugram, your primary responsibility will include reviewing various R&D documents such as stability data, analytical reports, method qualification reports, method verification reports, method validation protocols & reports, working standard/impurity standard profile, analytical data of pilot bio batches, and method transfers protocol & report. You will also be required to review lab events, deviations, change control, CAPA, and associated investigation reports before Technology Transfer. Additionally, you will support and participate in failure investigations to resolve root causes for issues related to systems and products developed within the R&D sites. You will visit AD Labs/Areas to ensure compliance with GDP & GMP standards and conduct audits of the Analytical Development department. It will be your responsibility to ensure that periodic activities as per the quality procedures are performed in a timely manner and collaborate with cross-functional and corporate teams for audit readiness. You will lead the assessment, tracking, and monitoring of identified actions as part of various corporate initiatives and support the operations team during corporate and external audits. Furthermore, you will review and approve product development data and specifications, in addition to performing any other duties assigned by the Functional Head. Your role will be critical in maintaining the quality standards and compliance within the R&D Quality-CMC QA department, contributing to the overall success of Sun Pharmaceutical Industries Limited.,