Executive – Quality Control (QC) – OSD Formulation
Key Responsibilities:
Perform analysis of raw materials, in-process, finished products, and stability samples.
Operate and maintain analytical instruments (HPLC, GC, Dissolution, UV, IR).
Prepare and review analytical documents, COAs, STPs, and SOPs.
Ensure compliance with cGMP, GLP, and regulatory requirements.
Handle OOS/OOT, deviations, and investigation reports.
Participate in method validation, calibration, and documentation activities.
Maintain lab records, samples, and ensure data integrity.
Qualification & Experience:
B. Pharm / M. Sc
6–8 years of QC experience in OSD formulation plant.
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