Masters Degree in Pharmacology, Life Sciences from a recognized university. Experience in the Research field and scientific writing. Candidates with proficiency in computer application will be preferred.
Audit exposure in USFDA/ EUGMP approved company. Exposure of Material Handling / Electronic Batch Record filling and review / Good Knowledge of SAP System & Their T Codes for PPPI / Machine Alarms handling / QMS / Deviation / Change Control / SOP / Daily Reports Preparation/ Manpower Handling.
Conduct thorough visual inspections of products to identify defects, damages, or inconsistencies, ensuring they meet company quality standards before packaging as per SOP.