Healthcare Leader
In India 
Dr. Reddy brings over 17 years of extensive experience in the pharmaceutical industry, having held various pivotal roles in top-tier pharmaceutical companies. His diverse background spans the entire product lifecycle, from concept to commercialization, across multiple dosage forms.
Educational Achievements:
Areas of Expertise:
Key Strengths:
Research Focus:
Dr. Reddy's doctoral research focused on innovative approaches to sustained release formulations, specifically targeting:
This research has contributed significantly to advancements in controlled release drug delivery systems, enhancing patient compliance and treatment efficacy.
Industry Impact:
Throughout his career, Dr. Reddy has played a crucial role in various stages of pharmaceutical development, from initial concept to final commercialization. His expertise in formulation design and deep understanding of drug delivery mechanisms have been instrumental in bringing numerous successful products to market.
Dr. Reddy's wealth of experience and academic achievements position him as a valuable asset in the pharmaceutical industry, driving innovation and excellence in drug formulation and delivery.
Mr. Lakshmikanth is an MBA graduate from BML Munjal University and has worked in various positions from in the pharmaceutical industry from the past 5 years
Educational Background:
MBA in Accounting and Finance from BML Munjal University
Professional Expertise:
Career Highlights:
Key Strengths:
Rabi Shankar Das is the General Manager and Quality Head for the Pellets Manufacturing Site. He has a Master’s Degree in Science (Biochemistry) and possesses more than two decades of expertise in Pharmaceutical Quality and compliance. He is an ISO certified Lead Auditor and trained CAPA investigator. He has worked with Leading Pharmaceutical Companies like Johnson & Johnson (Jenssen Pharmaceutical), Fresenius Kabi, Ferring Pharmaceutical, Laurus Labs, Glukem Biocare at various positions in the Quality Organization. He is instrumental in uplifting the Compliance status of the Organization with in-depth understanding of the dynamic challenges of Regulatory environment and cGMP expectations. He is responsible for implementing Quality Management system, hosting Regulatory inspections, and Customer Audits. He has strong focus on Product Quality improvement, customer-oriented process optimization and product life cycle management.
Senior Manager and Project In-charge
K. Mahendar Reddy brings over 12 years of extensive expertise in Pharmaceutical Engineering and Projects to his role as Senior Manager and Project In-charge for the Pellets Manufacturing Site. With a solid foundation in Mechanical Engineering, evidenced by his B.Tech degree, Mr. Reddy has built an impressive career working with leading pharmaceutical companies including Natco Pharma, Sri Krishna Pharmaceutical, Dr. Reddy's Labs, Mars Therapeutics, and Lara Drugs. Throughout his career, Mr. Reddy has held various positions within Engineering Departments, honing his skills and expanding his knowledge base. His primary responsibilities include implementing robust engineering and project management systems, hosting engineering inspections, and overseeing designs, projects, and machinery. Mr. Reddy's strong focus on pharmaceutical engineering design and project management has been a hallmark of his professional journey. Mr. Reddy's areas of expertise span a wide range of critical functions in pharmaceutical manufacturing. He is highly skilled in pharmaceutical machinery maintenance, equipment qualification and validation, and calibration processes. His proficiency extends to GMP documentation in regular processes, utility maintenance, and HVAC systems and validation. This comprehensive skill set enables him to ensure smooth operations and regulatory compliance in complex pharmaceutical manufacturing environments. With his unique combination of mechanical engineering background and extensive pharmaceutical industry experience, K. Mahendar Reddy is a valuable asset in managing intricate engineering projects and maintaining stringent regulatory compliance. His expertise continues to contribute significantly to the efficiency and quality of pharmaceutical manufacturing processes.