PharmaChemPro

Assistant Manager Quality Control

Mar 2024 - Present • 2 yrs 4 mos

Assistant Manager Quality Control with practical experience in pharmaceutical manufacturing and analytical laboratories. Responsible for the testing and evaluation of raw materials, packaging materials, in-process samples, finished products, and water samples according to approved specifications and standard testing procedures. Experienced in analytical techniques including HPLC, UV-Visible Spectrophotometry, pH measurement, dissolution testing, assay determination, and routine laboratory analysis. Skilled in performing analytical calculations, reviewing test results, investigating laboratory deviations, and ensuring compliance with quality standards and regulatory requirements. Actively involved in the preparation, review, and implementation of SOPs, STPs, analytical reports, specifications, and laboratory documentation. Supported method validation, method verification, equipment qualification activities, and GMP compliance programs within the quality control department. Key responsibilities include sample management, data review, result interpretation, laboratory record maintenance, calibration coordination, documentation control, and ensuring adherence to data integrity principles. Worked closely with production, quality assurance, and regulatory teams to maintain product quality and support continuous improvement initiatives. Achievements include successful execution of analytical testing projects, preparation and revision of quality control documentation, implementation of laboratory best practices, support in regulatory compliance activities, and maintenance of accurate and reliable analytical records. Demonstrated strong problem-solving abilities, attention to detail, and commitment to quality while meeting deadlines in a regulated pharmaceutical environment. Dedicated to delivering accurate, high-quality, and professional work while maintaining confidentiality, integrity, and client satisfaction.

Senior Executive Research and Development

Feb 2022 - Present • 4 yrs 5 mos

Research and Development professional with a strong academic background in Chemistry and practical experience in pharmaceutical product development, analytical method development, and laboratory research activities. Experienced in conducting scientific investigations, experimental studies, formulation support, analytical testing, and technical documentation within a regulated pharmaceutical environment. Participated in research projects involving method development, method optimization, and analytical evaluation of pharmaceutical products. Performed laboratory testing using analytical instruments such as HPLC and UV-Visible Spectrophotometry to support product development and quality assessment activities. Responsible for data collection, result interpretation, trend analysis, and preparation of scientific reports. Demonstrated expertise in experimental design, problem-solving, scientific literature review, and research documentation. Assisted in the development and improvement of analytical procedures, testing methodologies, and laboratory practices to enhance efficiency, accuracy, and reliability of results. Prepared and reviewed technical documents including research reports, protocols, SOPs, STPs, specifications, analytical methods, validation documents, and scientific presentations. Worked collaboratively with cross-functional teams including Quality Control, Quality Assurance, Production, and Regulatory Affairs to support product development objectives and regulatory compliance requirements. In addition to pharmaceutical research experience, developed expertise in scientific writing, technical content development, educational material preparation, chemistry tutoring, and research-based communication. Capable of transforming complex scientific concepts into clear, accurate, and professional documentation for academic, industrial, and commercial applications.