Lead formulation development for new products and reformulation of existing products in line with QbD principles.
Monitor and evaluate stability studies, ensuring accurate data compilation and reporting.
Prepare and review Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR).
Execute process optimization, submission batches, and process validation activities.
Plan, coordinate, and monitor Bioequivalence (BE) studies.
Support regulatory submissions and respond to regulatory queries.
Assist in Continuous Process Verification (CPV) and product lifecycle management activities.
Coordinate projects and maintain effective communication with internal and external stakeholders.
Mentor, train, and develop junior team members.
Age 30 to 40 years
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