Roles and ResponsibilitiesConduct quality control analysis using HPLC, GC, UV, spectrophotometer, sterile techniques, and other relevant methods.Ensure compliance with USFDA, GMP, GLP regulations during regulatory audits.Develop and maintain SOPs for laboratory operations and testing procedures.Collaborate with cross-functional teams to resolve quality issues and improve processes.Perform stability studies on APIs and finished products as required.Desired Candidate Profile2-7 years of experience in a pharmaceutical industry setting with expertise in QC analysis.MS/M.Sc(Science) degree in Chemistry or related field; Strong understanding of analytical instruments such as HPLC, GC, UV spectrometer etc., and ability to operate them effectively.