Team Member - In Process QA

Dr. 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 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.

Responsibilities

Responsibilities; Performing of in process activities such as Line Clearance, in process checks, AQL and sampling in manufacturing operations.; Batch record review and handling of exceptions generated through PAS-X; Review of in process labelling and status of material.; To ensure cGMP (Current Good Manufacturing Practices) compliances.; To Follow Safety, Health and Environmental procedures and practices.; Review and approval of Equipment Specification Checklist in PAS-X.; To ensure the compliance of the functions related to PAS-X activities and their relevant records as per procedures.; To impart training to the personnel involved in PAS-X activities and also attend the Trainings wherever applicable.; Collection of Swab sample for cleaning validation activities; Collect water sample for monitoring of water quality.

Requirements

Educational Qualification; B.Pharm