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 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 Required Experience: 2 - 5 years
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