* **1. JOB OBJECTIVE** * Ensure product quality by meeting physicochemical specifications during stability studies, complying with accelerated and long-term stability programs for pilot and finished products. * **2. GENERAL FUNCTIONS AND SPECIFIC RESPONSIBILITIES** * Ensure results of stability studies for finished products. * Perform stability studies according to established technical specifications and analytical methodologies. * Report analysis results from stability studies. * Develop long-term, accelerated, and in-use stability study protocols. - * Organize and maintain samples under required conditions for the corresponding stability study. * Coordinate, supervise, and record temperature and humidity of stability chambers. * Attend general training sessions and provide internal training to area personnel on technical aspects and the quality system, as well as undergo corresponding evaluations. * Support the development and updating of procedures, protocols, and work instructions within the section. * Assist in the analysis of raw materials, in-process products, and finished products. * Report any detected non-conformities or doubts to the area supervisor. * Perform other duties assigned by the immediate supervisor and/or the Quality Control Manager. * **3. JOB PROFILE EDUCATION** * Professional degree and licensed pharmacist qualification or bachelor's degree in pharmaceutical chemistry. * **TRAINING** * - Knowledge of GMP and GLP * - Desirable knowledge of ISO 17025:2017 standard * - Proficiency in office software * - Experience handling HPLC, GC, IR, and other equipment * - Desirable experience in stability studies for pharmaceutical products * **SKILLS** * - Planning and organization - * Analytical thinking * **EXPERIENCE** * - Minimum of 2 years of experience in similar roles within the pharmaceutical industry is desirable. Job type: Full-time Salary: S/.1,800.00 - S/.2,000.00 per month Work location: On-site