Seeking a Quality Chemist for a pharmaceutical manufacturing unit to perform analysis of raw materials, in-process, and finished products using HPLC, GC, UV, and wet chemistry methods. Ensure GMP/GLP compliance , handle OOS/CAPA , maintain instruments, and support audits (WHO/USFDA/ISO). Qualification: B.Sc./M.Sc. Microbiology 1 to 3 years of QC/QA experience.
Formulation development and optimization for liquids and tablets Execute lab/pilot/commercial batches with complete documentation Perform stability studies and analytical/physical testing Troubleshoot formulation and manufacturing issues to improve product quality Support technology transfer and scale-up to production Ensure compliance with cGMP / WHO-GMP / regulatory requirements Maintain BMR, BPR, SOPs and technical reports Coordinate with QA/QC/Production/Regulatory for smooth execution of projects