




Job Summary: We are seeking a qualified Documentation Analyst with experience in the pharmaceutical industry to manage and control product documentation and dossiers. Key Highlights: 1. Essential role in documentation control within the pharmaceutical industry. 2. Knowledge of GDP, GMP, GLP, GCP, and NOM-059 required. 3. Proficiency in Statistics and Change Controls is mandatory. A solid Mexican pharmaceutical group with over 46 years in the pharmaceutical market We seek your talent as: **DOCUMENTATION ANALYST** **Requirements:** * Education: Degree in Pharmacy and Biochemistry (QBP), Food Chemistry (QFB), Biomedical Engineering (IBI), Industrial Food Engineering (IF), or related field. * Experience: Minimum 1 year as a Documentation Analyst Chemist in the pharmaceutical industry. * Knowledge of GDP, GMP, GLP, GCP, NOM-059, etc. * Minimum 1 year of experience in handling and controlling documentation as stipulated by current regulations, and managing product dossiers. * **Mandatory proficiency in Statistics and Change Controls related to modifications of any documentation associated with manufactured products.** * Analytical and synthesis capabilities; timely and effective problem-solving skills. * Service-oriented attitude: Maintain constant communication with related departments and supervisors. * Follow up on any out-of-specification results, deviations, or quality risks. * Comply with the Quality Management System, standards, policies, and safety, hygiene, and environmental protection measures. * Verify that documentation is accurate and traceable. **We Offer:** ° Gross Monthly Salary ° Enhanced benefits including savings fund, grocery vouchers, and subsidized cafeteria service Work schedule: Monday to Friday, 09:00 AM to 06:00 PM Work location: Poniente 150 Vallejo


