Department Details

Role Summary

Urgent Requirement for Formulation Development - OSD role (Scientist / Senior Scientist)
•Handling Formulation Development - OSD / Solidi Orals
• Keeps abreast of current trends, practices, developments, and regulatory changes, which would affect products, procedures or formulation
• Execution of experiments timely in meticulous manner
Pharmaceutical Product/ Technology/Formulation Development for Drugs from conceptualization to proof of concept, technology transfer for regulatory filings and commercialization of drug products.
• Formulation Research Development as per Quality by design (QbD), Optimization of Drug Formulations using design of experiment (DoE).
• Drug product development of oral solid dosage forms for the global market.
• Complete documentation of the experiments, results and discussion on way forward with superiors.
• To ensure the adherence to all the EHS policies

Key Responsibilities

• Keeps abreast of current trends, practices, developments, and regulatory changes, which would affect products, procedures or formulation.
• Execution of experiments timely in meticulous manner.
• Pharmaceutical Product/ Technology/Formulation Development for Drugs from conceptualization to proof of concept, technology transfer for regulatory filings and commercialization of drug products.




• Formulation Research Development as per Quality by design (QbD), Optimization of Drug Formulations using design of experiment (DoE).
• Drug product development of oral solid dosage forms for the global market.
• Complete documentation of the experiments, results and discussion on way forward with superiors.
• Constructs experimental studies intended to provide supporting data or to resolve technical issues encountered during a project.
• Optimized formulations and process & Transferring technology
• Assist in resolving technical issues and drive the completion of investigations that affect the technical scope, makes recommendations for various options that would resolve the issue,
• Ensures the maintenance and/or adherence to positive laboratory practices and all safety regulations in manufacturing areas.
• execution of drug product development, scaleup, technology transfer, process development and process validation at cGMP standards manufacturing sites.
• Proposes and implements recommendations to processes and procedures designed to increase efficiency, safety, or quality
• Maintain current training records for required procedures
• To ensure the adherence to all the EHS policies

Educational Qualifications

Required Education Qualification:
Required Experience: 2 - 5 years

📌 SCIENTIST (India)
🏢 BIOCON PHARMA
📍 India