Roles & Responsibilities

- Develop and optimize sterile ophthalmic formulations, including ophthalmic solutions, suspensions, and emulsions.

- Conduct formulation development and process optimization at laboratory scale and support scale-up to pilot/production scale.

- Perform technology transfer of sterile dosage forms from R&D; to manufacturing sites.

- Coordinate with manufacturing, QA, QC, and other cross-functional teams during scale-up and technology transfer activities.

- Provide technical support and troubleshooting for commercial batches and manufacturing-related issues.

- Investigate and support resolution of OOS, OOT, deviations, process-related issues, and formulation-related problems.

- Participate in root cause analysis and implementation of corrective/preventive actions (CAPA).





- Prepare and review formulation and process-related documents such as MFR, BMR, development reports, stability protocols, and stability reports.

- Monitor stability studies and evaluate formulation/product performance.

- Ensure formulation development activities comply with GMP and applicable regulatory requirements.

- Visit different manufacturing sites as required for technology transfer, scale-up, troubleshooting, and commercial batch support.

- Maintain proper technical documentation and ensure timely completion of assigned R&D; projects.

- Work closely with cross-functional teams to ensure successful product development, scale-up, and commercialization.

📌 Formulation and Development Scientist (Mumbai)
🏢 Navlakha Management Services
📍 Mumbai