Job Responsibilities

• Perform chemical analysis of raw materials, packaging materials, in-process and finished pharmaceutical products, including products on stability, according to written methods or compendial methods as applicable using analytical techniques such as IR spectroscopy, UV-Vis spectroscopy, and chromatographic techniques.
• Prepare samples for analysis involving thorough cleanliness and complex steps for analysis using chromatographic techniques and analyze.
• Create and maintain laboratory record documentation (notebooks and computer-based), document exact steps followed during analysis execution, calculate and report results in a timely manner.
• Actively participate in method transfer activities between facilities within the organization or between organizations.

• Actively participate in and lead investigation of out-of-specification laboratory results, when required.
• Perform physical analysis involving complex techniques such as X-ray diffraction, DSC, Malvern mastersizer.
• Prepare and execute method transfer protocols, method verification/validation protocols as and when required.
• Interact effectively with multi cross-functional teams and work closely with other departments for preparation of regulatory filings.
• Comply with lab SOPs, GLP, GMP, and company safety requirements.
• Perform other related duties as assigned to meet departmental and company objectives.