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 good 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: M.Pharma