Scientist Job at Dr Reddy’s Laboratories | MPharm Graduates Apply Now
Dr. Reddy’s Laboratories is seeking a dynamic and experienced Scientist in Process Engineering to join its Integrated Product Development Organisation. This Scientist Job requires 3-5 years of experience in API Manufacturing and proven expertise in scaling up or down technologies to meet production demands. The scientist will be responsible for process optimization, conducting feasibility studies, performing laboratory validations, and executing the Technology Transfer of API processes to the plant, ensuring high reproducibility and compliance with quality and regulatory standards.
- Job Post: Process R&D Scientist
- Location: Hyderabad, Telangana, India
About the Company
Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company founded in 1984, driven by the purpose: “Good Health Can’t Wait.” With over 24,000 employees, the company operates research and development centres, manufacturing facilities, or commercial presence in 66 countries globally. Dr. Reddy’s is committed to accelerating access to affordable and innovative medicines, utilizing deep science, robust corporate governance, and progressive people practices. Through its “The Next and the New” strategy, the company aims to reach over 1.5 billion patients worldwide by 2030, emphasizing sustainability across people, planet, and purpose.
MPharm Job Description
We are seeking a dynamic and experienced Scientist in Process Engineering in Active Pharmaceutical Ingredient (API) development with proven expertise in scaling up or down technologies to meet production demands. Proficient in Process and Chemical Engineering, adept at troubleshooting complex projects, facilitating technology transfer, and optimizing operations.
Roles & Responsibilities of the MPharm Job
- You will be responsible to review of journals and patents.
- You will be responsible for feasibility study of the Process, Process Optimization, Lab Validations, Technology Transfer to plant and identify and evaluate the reaction parameters.
- You will be responsible for staying up to date with relevant scientific and technical developments. Execute experiments efficiently with high reproducibility.
- You will be responsible for interpretation of analytical and spectral data to ensure quality and regulatory compliance.
- You will be responsible to write technical development reports, Quality by Design (QbD) reports, justification reports and Drug Master Filing (DMF) filing related documents.
- You will be responsible to provide support in scale up batches execution and ensure process reproducibility at scale.
- You will be responsible for ensuring lab safety and process safety.
Educational Qualification
M.Sc/ M.Pharma
Minimum work experience
3-5 years of Experience in API Manufacturing
Skills & Attributes:
Technical Skills
- Have work experience on Process scale up of Active Pharmaceutical Ingredients.
- Experience in Process Optimization (Manufacturing).
- Experience in Process Intensification.
- Experience in Operational Excellence.
- Experience in Chemical Process Engineering.
- Experience in Technology Transfer.
Behavioral Skills
- Excellent communication and interpersonal skills.
- Strong analytical and problem-solving abilities.
- Ability to work collaboratively with own team and cross-functional teams.
