·Responsible for manufacturing solid dosage forms as specified by SOP, cGMP
·Conducted routine analysis of raw materials, in- process products and finished products to ensure in compliance with cGMP, GLP, FDA guidelines
·Analyzed samples using analytical methods for physical testing, assay, dissolution etc.
·Performed formulation optimization technique for better quality product development
·Prepared and reviewed batch manufacturing records
·Executed validation protocols and conducted validation studies in accordance with applicable cGMP and company SOPs
·Prepared GMP compliant test samples to predetermined specifications