Job Description

Key Responsibilities: Perform routine and non-routine chemical analyses of raw materials, in-process samples, and finished products using various laboratory instruments (e.g., HPLC, GC, UV-Vis, FTIR). Calibrate, maintain, and troubleshoot laboratory instruments to ensure accurate and reliable results. Prepare and review Standard Operating Procedures (SOPs) for analytical methods and ensure compliance with quality standards. Analyze data from testing and document results in reports, ensuring proper record-keeping and traceability. Conduct stability studies and product testing to ensure that products meet specifications. Work closely with production teams to resolve any quality-related issues and recommend corrective actions. Assist in the development and validation of new analytical methods. Ensure compliance with Good Laboratory Practices (GLP) and relevant regulatory requirements (e.g., GMP, ISO). Perform equipment maintenance and troubleshooting to ensure continuous operation of testing instruments. Assist in the preparation for internal and external audits and inspections. Qualifications: Bachelors degree in Chemistry, Biochemistry, or a related field. Proven experience (2+ years) in a Quality Control role within a laboratory or pharmaceutical/chemical industry. Familiarity with lab instruments such as HPLC, GC, UV-Vis spectrophotometer, and other analytical techniques. Strong understanding of GLP, GMP, and regulatory standards. Excellent attention to detail and ability to work independently. Strong analytical and problem-solving skills. Good communication and documentation skills. Ability to work under pressure and meet tight deadlines.