Process Development 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 to Conduct strategy evaluations to design and optimize pharmaceutical processes, ensuring efficient and cost-effective development.
• You will be responsible to Calculate batch sizes for both early development and commercial production, considering critical parameters and quality standards.
• You will be responsible to Lead process development activities for oral solid formulations, from concept to commercialization, including the design of experiments and formulation strategies.
• You will be responsible to Perform scale-up calculations and execute scale-up processes to ensure successful transition from lab-scale to production-scale.
• You will be responsible to Handle exhibit batches, coordinating activities and documentation to meet regulatory requirements and project timelines.
• You will be responsible to Prepare and maintain technical documentation, including development reports, process validation protocols, and regulatory filings.
• You will be responsible to Collaborate with cross-functional teams to drive process improvements, troubleshoot issues, and ensure product quality and consistency.
• You will be responsible to Stay updated with industry trends and regulatory guidelines, incorporating best practices and innovative technologies into the development process.
  

Qualifications

Educational qualification:

• Experience in process optimization, development and troubleshooting in relevant dosage forms or technologies
• Hands-on experience in end-to-end scale up
• Depth understanding of process techniques & equipment knowledge 
• Knowledge on Deficiency management and product validations.
• Experience in manufacturing process improvement.
• Experience with oral solid formulations.

Behavioral Skills

• 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.
  

Additional Information

About the Department

Integrated Product Development Organisation

Benefits Offered