Team Lead - Visual Inspection

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.

Responsible for end to end management of drug product visual inspection operations (Manual and Automated) as per SOPs, Batch Manufacturing Record, QMS item and cGMP norms. Responsible for total compliance of QMS elements.

Responsibilities

To coordinate team shift allocation according to the planned schedule and ensure timely approval of employee leave requests.; To monitor, track and review QMS elements (Change controls, CAPA, incident management, SIR, market complaints etc.) and ensure the closure of the same on time.; To review and compliance of Audit points.; To plan optical inspection operations in compliance with delivery, quality and with safety.; To involve in visual inspection projects activities (to prepare URS, involving in the FAT, SAT & equipment Qualification) for current and ongoing projects.; To review and execute/ support the process validation protocols and its reports.; To review the revised batch production records MFRs SOPs etc.; To follow ensure clean room behaviors techniques team members.; To identify reporting unsafe conditions acts.; To coordinate packaging qualification activities and associated documentation in compliance with applicable procedures.; Training staff member’s relevant cGMP aspect operations.; To handle any other work assigned L+I Department charge.

Requirements

B.Sc/B. Pharma/M.Sc/M.Pharma