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SCIENTIST

0.00 to 10.00 Years   India   07 Jun, 2024
Biocon
Job LocationIndia
EducationNot Mentioned
SalaryNot mentioned
IndustryNot mentioned
Functional AreaNot Mentioned
EmploymentTypeFull-time

Job Description

Department DetailsRole SummaryUrgent 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 QualificationsRequired Education Qualification: M.Pharma Required Experience: 2 - 5 years

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