Responsibilities
List of Responsibilities I Job Functions:
- Timely validation of analytical methods of the drug products and API (intermediates and key starting material) for the drug products I drug substances to be filed globally. This role necessitates understanding of cGMP requirements and valuable technical knowledge to validate analytical methods and establish their suitability for the intended use.
- Documentation of data as per laid down procedures during execution of validation experiments
- Interaction with Internal compliance group/R&D; quality-CQA to answer their queries during review of validation documents. .
- Transfer of analytical methods at different plant locations before exhibit batches.
- Ensuring cleanliness in GMP area at all times in terms of proper labeling at all designated places and arrangement of chemicals.
- The role requires continuous up gradation in terms of regulatory and GMP requirements pertaining to method validations and attending SOP / Compliance related trainings.
- Any other responsibilities assigned from time to time orally or in writing.

📌 Executive (Gurugram)
🏢 SUN PHARMA
📍 Gurugram