Formulation 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 discussion and planning strategies for product development, executing them and recording them in E-Lab notebook.
• Identify and proactively discuss potential challenges along with possible way forward.
• Collaborate and coordinate with analytical team for batch analysis followed by data analysis from time to time.
• Relevant documentations for license application and executions of pilot plant batches, stage gate clearances from time to time.
• Biweekly present project status to the delivery manager.
• Coordinate with process teams for optimization trials, plant presentations, preparation and review of plant documents and scale up the product from lab scale to exhibit scale/commercial scale.
• Support filing the product with PDR, support deficiency responses and submission of exhibit batch samples for pharmaceutical examinations/clinical studies, etc.
• Follow company systems and processes compliance to safety and quality.
  

Qualifications

Educational qualification:

Skills & attributes:

• Having worked on Differentiated Solid Oral Dosage Forms, platform technologies, hands on experience on modified release pellets and matrix formulations can be preferred.
• Hands on experience on lab scale and plant scale equipment's used in manufacturing of Oral solids and liquid formulations.
• Shouldering end-to-end responsibilities of product development team.
• Demonstrates data analytical and problem-solving skills.
• Know how on ICH guidance's, regulatory requirements for regulated and semi-regulated markets, cGMP and cGLP practices.

Behavioral

• Overall communication and presentation skills.
• Strong analytical and problem-solving abilities.
• Result oriented.
• Ability to work collaboratively with own team and cross-functional teams.
• Committed to continuous learning.
  

Additional Information

PhD (Pharmaceutical Science)