1. Formulation Development
Lead development of solid and liquid non-sterile dosage forms
Conduct and oversee pre-formulation studies and excipient compatibility.
Optimize formulations for bioavailability, stability, and cost efficiency.
2.Scale-Up & Tech Transfer
Lead scale-up activities from lab to pilot.
Troubleshoot formulation issues during manufacturing.
Ensure smooth technology transfer to production.
3.Regulatory & Compliance
Ensure compliance with GMP, ICH, WHO, and local regulatory guidelines.
Support regulatory submissions, variations, and responses to authority queries.
Maintain accurate development documentation and SOPs.
4. Continuous Improvement & Innovation
Apply QbD and risk-based approaches to formulation development.
Improve existing products to reduce cost, failures, or variability.