Team Member - Production QMS

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.

Job Summary

• You will be responsible for overseeing the compliance activities in day-to-day production activities.

• You will be responsible for the incident/deviation brainstorming, investigation and closure.

• You will be responsible for implementation of CAPA actions and change proposal actions.
• You will be responsible for guiding and coaching employees, monitoring their productivity, and overseeing regular equipment safety and maintenance.• You will be responsible for review of Documentations, BMR (Batch Manufacturing Records), BPR (Batch Production Records) and Logbooks.• You will be responsible for ensuring product quality by maintaining cGMP (current Good Manufacturing Practices).• You will be a training coordinator through LMS (Learning Management system).• You will be responsible for generating the process order number.

Qualifications

Educational qualification

• Knowledge of Pas|X, isolator operation, lyophilizer, vial filling.
• Knowledge and experience in injectable manufacturing and packing.• Experience in Liquid and lyophilized product manufacturing and packing.• Good understanding of GMP and good laboratories practices.

Behavioural skills

Additional Information

About the DepartmentGlobal Manufacturing Organisation (GMO)