Process R&D Scientist

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 executing experiments, collecting and interpreting data to facilitate smooth process development. This role involves collaborating with cross-functional teams, utilizing Quality by Design (QbD) principles.
• You will be responsible to demonstrate successful process scale up to ensure smooth execution of T&V Batches on time.
• You will be responsible to prepare documents required for T&V batch at plant.
• You will be responsible to prepare Process optimization report & filing documents.
• You will be responsible to analyse data and provide support in answering process related deficiencies ensuring on time response to regulatory agencies.
• You will be responsible to develop process capabilities within team, train new joinee /freshers. Willingness to imbibe young talent and support in the initial stages.
  

Qualifications

Educational qualification:

• Experience in the development/ scale up/ technology transfer of products in relevant dosage forms or technologies.
• Understanding of pharmaceutical process selection
• Ability to prepare technical protocols and reports.
• Experience in process Engineering, Quality by Design (QbD) principles and risk assessment approaches.
• Knowledge of International Council for Harmonisation (ICH) guidelines related to Product development or Process Development.
• Experience in Formulation Development understanding of execution methodology (based on Critical Material Attributes, Critical Quality Attributes of products.
• Experience in Analytical Research and knowledge on interpretation of the data.

Behavioral

• Excellent communication and interpersonal skills.
• Strong analytical and problem-solving abilities.
• Performance oriented and good at building, leveraging relationship.
• Ability to work collaboratively with own team and cross-functional teams.
• Committed to Learning & Coaching the team.
  

Additional Information

About the Department

Integrated Product Development Organisation

Benefits Offered