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.

We are seeking a highly skilled Process Scientist API (Active Pharmaceutical Ingredient) to join our team in Hyderabad, India. In this role, you will be responsible for developing, optimizing, and scaling up API manufacturing processes to ensure efficient and high-quality production of pharmaceutical ingredients.

• Design, develop, and optimize API manufacturing processes from laboratory scale to commercial production
• Conduct experiments and analyze data to improve process efficiency, yield, and product quality
• Troubleshoot process issues and implement solutions to enhance overall performance
• Collaborate with cross-functional teams to ensure smooth technology transfer and scale-up of API processes
• Prepare comprehensive technical reports and documentation for internal and regulatory purposes
• Stay updated on current Good Manufacturing Practices (GMP) and regulatory requirements in the pharmaceutical industry
• Participate in process validation activities and support regulatory filings
• Mentor junior scientists and contribute to the continuous improvement of the department
  

Qualifications

• Ph.D. or Master's degree in Chemistry, Chemical Engineering, or a related field
• 3-5 years of experience in API process development or a related field within the pharmaceutical industry
• Extensive knowledge of API manufacturing processes and pharmaceutical industry regulations
• Strong expertise in process development, optimization, and scale-up techniques
• Proficiency in analytical techniques and instrumentation commonly used in API development
• Excellent problem-solving and troubleshooting skills with a detail-oriented approach
• Familiarity with Good Manufacturing Practices (GMP) and pharmaceutical industry standards
• Strong data analysis and interpretation skills
• Proficiency in using laboratory equipment and relevant software
• Excellent written and verbal communication skills
• Ability to work efficiently in a fast-paced, collaborative environment
• Experience with tech transfer and process validation is preferred
  

Additional Information

About the Department

Integrated Product Development Organisation

Benefits Offered