Required Education/Qualifications/Skills
- M.Sc./M. Pharma in Pharmaceutical Analysis/Chemistry with around 4-6 years of experience in analytical R&D for pharmaceutical formulations
Main Accountabilities
- Routine analysis & Stability Analysis (assay, RS, dissolution, water content etc.) of R&D formulation projects (solid & liquid orals, injectables)
- Daily calibration of pH meters, balances etc.
- Stability sample management (loading & withdrawal as per stability plan)
- Preparation of Stability Reports & other protocol based study reports for assigned projects, as applicable
- Hands-on experience of analytical instrumental techniques (HPLC with chromatographic software etc.)
- Assisting analytical method development/validation/method transfer activities, as per need
- Supporting other assigned lab responsibilities for GLP compliance
Performance Indicators:
- Timely execution of assigned responsibilities of services team
- Maintaining GLP conditions in lab
- Ensuring adherence to GDP
