
Detail-oriented Senior Specialist with over 6 years of expertise in analytical method development, validation, troubleshooting, and instrument handling. Strong background in HPLC and GC techniques related to active pharmaceutical ingredients, complemented by a solid understanding of USP and ICH guidelines, along with laboratory quality systems. Proficient in preparing comprehensive validation protocols and reports while ensuring strict adherence to cGMP compliance standards. Proven track record of delivering high-quality results in fast-paced environments underscores a commitment to excellence within the pharmaceutical industry.