Lead MSAT- FTO

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

Qualifications

Educational qualification:

* Knowledge of working on complex Equipment ( High Pressure Homogenizer, Aseptic ANFD, SKID process Mfg processes, Microfluidizer, Homogenizer, Bead mill in aseptic methodology

* Knowledge on Sterile Filtration, Filling, Lyo

* Knowledge on Media fill strategy finalization.

* Capable to Review and/or prepare PID/FS/FDS etc

*Extensive knowledge of continual process robustness, equipment Installation & qualifications, cleaning procedures, and safety risks.
• Proven ability to oversee the closure of incidents and investigations with effective CAPA and addressing root causes to prevent repeat incidents.• Strong focus on continuous improvements in quality, production capacity, batch cycle times, yield improvements, technologies, and waste reduction.• Ability to develop common solutions for platform issues impacting multiple sites and preparing risk assessments for any modifications or changes.• Proven experience in assessing opportunities and implementing changes related to scale-up and modifications in processes/equipment at various stages of product development.

Behavioural skills

Additional Information

About the Department

Integrated Product Development Organisation

We integrate our deep science capabilities and cutting-edge technology to develop innovative, accessible and affordable therapies for patients worldwide. We are a science-driven, innovation-focused pharmaceutical company committed to accelerating access to healthcare solutions to patients around the world. We have End to end capabilities in API, Formulations, Clinical, Intellectual Property and Regulatory Affairs. We are serving 55+ markets including USA, Canada, Europe, China, LATAM, ASEAN and all Emerging Markets with innovative and generic products ranging from Active pharmaceutical ingredients (API), Oral formulations, Parenteral (Injectables, Opthalmics) & Other dosages
Our product development efforts drive a portfolio of more than 1,000 products Enabled by our robust R&D team consisting of more 200 scientists and functional experts and more than 150 doctorates, we have filed 1,071 patents and also published over 1,000 papers for peer review over the years.

Benefits Offered