.Company DescriptionDr. Reddy's Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can't Wait.We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries.For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further and to build the future.'The Next and the New' is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose.Dr Reddy's maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic protected by applicable law(s).Job DescriptionJob SummaryWe are seeking an analyst for the Quality Control team who will be responsible for analysing assigned samples and conducting authorized transactions. The role involves following SOPs (Standard Operating Procedures), STPs (Standard Testing Protocols), GLP (Good Laboratory Practices) and safety standards. The ideal candidate will maintain 5S practices, and handle additional responsibilities assigned by the team leader.Roles & ResponsibilitiesYou will be responsible for adhering to GLP (Good Laboratory Practices) and safety practices, and ensuring compliance with the SOP (Standard Operating Procedure).Your responsibilities include analysis of samples as assigned by the group leader, ensuring adherence to relevant SOPs and Standard Testing Protocols (STPs), and following online documentation and calculation practices.You will also be responsible for authorized transactions in SAP and LIMS (Laboratory Information Management System), as well as the online reporting of any Out-of-Specification (OOS), Out-of-Trend (OOT), and incidents to the group leader.You will be responsible for verifying that analytical results are conforming with specification limits.You will maintain and monitor 5S practices in the laboratory, perform sample management for the team and handle any other responsibilities assigned by the team leader