.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 (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 transparency.Dr Reddy's maintains a work environment free from discrimination and is an equal opportunity employer.
We are committed to employing & nurturing 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 DescriptionJob SummaryWe are seeking an individual to lead the validation and analytical method transfers for pharmaceutical materials, manage incidents and investigations, approve documents, and ensure laboratory compliance with practices and cleanliness.
The role involves procurement of laboratory requirements, instrument qualifications, and calibration.Roles & ResponsibilitiesYou will be responsible for validation and analytical method transfers of IP (In-Process), FP (Finished Product), API (Active Pharmaceutical Ingredient), Excipients and Packing materials.You will initiate and investigate CRN (Change Request Notice), Incidents, OOT (Out of Trend) and OOS (Out of Specification).You will be responsible for approval of STPs (Standard Testing Procedures), Specifications, SOPs (Standard Operating Procedures), Protocols and Analytical test reports.You will ensure Good laboratory practices, Safety practices, Good documentation practices and ensure the cleanliness of the laboratory