Company DescriptionDr. Reddys 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 Cant 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 (the next steps) and to build the future (the new bets).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 - helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparencyDr Reddys 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 or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization.Job Summary
We are looking for an individual for the Analytical Research and Development team.Roles & Responsibilities
Review of relevant literatureQualification of reference standard/working standardsDevelop analytical methods, conduct validations of these methods and transfer method to QCPrepare Method development and method validaiton reports.Do online sample analysis for product development.Procure chemicals, solvents, columns, etc..Maintain lab equipment's as per GLPUnderstand the safety and environment aspectCalibrate the instruments according to the calibration schedule and follow GLP and SOP's.Keep the work area clean and the laboratory under controlled temperatureMaintain the documents well.QualificationsEducational qualification: M.Sc ChemistryMinimum work experience: 5-8 years experience in operating chromatographic instruments like HPLC, GC and wet analysisSkills & attributes:
Technical Skills
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