Formulation & Development Officer Job Vacancies in Nashik

  • 10 - 20 yrs
  • 7.0 Lac/Yr
  • Nashik
Formulations Formulation & Development Officer Formulation Scientist Research and Formulation
Key ResponsibilitiesFormulation Design & Optimization: Lead the development of robust pharmaceutical dosage forms (Oral Solids, Liquids, Topicals, or Sterile Injectables). Apply Quality by Design (QbD) principles and execute Design of Experiments (DoE) to optimize formulation parameters and process steps.Pre-formulation & Compatibility Studies: Oversee critical physical and chemical characterizations, including API-excipient compatibility studies, solubility enhancement, and solid-state characterization.Technology Transfer: Manage the seamless scale-up and technology transfer of developed formulations from lab-scale to pilot plant and final commercial manufacturing sites. Troubleshoot scale-up issues directly on the production floor.Regulatory Dossier Support: Direct the compilation of technical documentation required for regulatory filings, including Product Development Reports (PDR), master formula records, and stability data protocols matching CTD/eCTD formats.Stability Testing Supervision: Oversee formulation stability trials according to ICH guidelines to determine product shelf-life and evaluate degradation pathways under accelerated and long-term conditions.Team & Lab Management: Lead, mentor, and evaluate a dedicated team of F&D scientists and research associates. Ensure strict laboratory safety compliance, chemical inventory tracking, and calibration of R&D equipment.
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  • 0 - 1 yrs
  • 3.0 Lac/Yr
  • Nashik
Research and Formulation Formulation Development Formulations Formulation & Development Officer
Key Responsibilities1. Pre-formulation StudiesCharacterization: Testing the raw API for physical and chemical properties like solubility, pH stability, and melting point.Compatibility: Conducting studies to see if the drug reacts negatively with certain excipients or packaging materials.2. Product Design & OptimizationRecipe Creation: Designing different versions of a drug (prototypes) to find the one with the best stability and bioavailability.DoE (Design of Experiments): Using statistical software to systematically test different ingredient ratios to find the Goldilocks formula.3. Stability & Quality TestingShelf-Life Testing: Placing batches in Stability Chambers to see how they react to extreme heat, humidity, and light over time.Dissolution Profile: Testing how quickly a tablet dissolves in a simulated stomach environment to ensure the drug is released correctly.4. Scale-Up & Technology TransferLab to Factory: Moving a formula that worked in a small beaker to large-scale machines that produce millions of tablets.Troubleshooting: Solving real-world manufacturing issues like tablets sticking to the machine or capsules becoming brittle.
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