F&D_IND_RA

Job Purpose

Key Responsibilities

• Design and develop solid (tablets, capsules) and liquid (syrups, suspensions) dosage forms.
• Conduct pre-formulation studies, prototype development, and scale-up trials.
• Optimize formulations for stability, bioavailability, and manufacturability.
• Develop innovative nutraceutical formulations aligned with market trends and therapeutic needs.
• Evaluate functional ingredients, excipients, and delivery systems for efficacy and safety.
• Prepare and review technical documentation for domestic regulatory submissions (FSSAI, CDSCO, etc.).
• Ensure adherence to regulatory guidelines and pharmacopeial standards.
• Design and execute stability protocols as per ICH guidelines.
• Analyze stability data and prepare reports for product registration and shelf-life determination.
• Support scale-up and technology transfer to manufacturing units.
• Collaborate with cross-functional teams including QA, QC, RA, and Production.
• Maintain comprehensive records of formulation trials, batch manufacturing records, and development reports.
• Prepare product development reports and dossiers for internal and external audits.
  

Desired Candidate Profile

• Education: M.Pharm / M.Sc. in Pharmaceutics or related field
• Experience: 3–6 years in formulation development for domestic market
• Hands-on experience in solid and liquid dosage forms
• Knowledge of nutraceuticals and functional ingredients
• Familiarity with domestic regulatory frameworks
• Proficiency in stability study design and documentation
• Strong analytical and problem-solving skills