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 positive 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 pertainingto method validations and attending SOP / Compliance related trainings. Any other responsibilities assigned from time to time orally or in writing. We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.

📌 Executive (India)
🏢 Sun Pharmaceuticals
📍 India