September 2025

Handling the Incidents / Deviations, Out of Trends, Out of Specification including investigations, Corrective and Preventive actions follow up and closure. Monitoring of analytical activities in Quality control laboratory.

Stallion Laboratories incorporated in 1988 as an integrated private sector Pharmaceutical Formulation Manufacturer, has acquired an unmatched record of managing niche product in formulations with a WHO GMP approved production facility

Responsible to perform routine analysis for Domestic and EMB market. Perform analytical method development for various dosage forms.

Seeking an exceptional leader to Head Pharmacovigilance and Medical Affairs including medical information function for Dr. Reddys North America Generics and affiliates as well as Dr. Reddys Canada

M.Sc. / B. Pharma. Experience in QC department of a pharmaceutical organization with knowledge of latest regulatory standards and compliance norms.

Exposure of analysis tor Finished Products. Stability Samples. Raw Materials & Packaging Materials.Having Knowledge of Analytical Method Validation, Verification & Method Transfer. Having skill for data interpretation, troubleshooting.Pharma knowledge of Solid orals & Quality process.

Degree in Pharmacy or Life Science, Medical, PharmD or related discipline (minimum M.Pharm or MSc or equivalent degree), higher degree preferable

Develop and execute quality and compliance monitoring activities for PS processes within area of expertise to support a robust GVP Quality Management System.

Develop and present key Competitive Intelligence deliverables for multiple internal business partners, primarily R&D, Commercial, and Legal stakeholders