Documentation Analyst

Description

Job Summary: We are seeking a qualified Documentation Analyst with experience in the pharmaceutical industry to manage and control documentation, ensuring regulatory compliance. Key Highlights: 1. Minimum 1 year of experience in pharmaceutical documentation 2. Knowledge of GPD, GMP, GLP, GCP, NOM-059, and dossier management 3. Mandatory proficiency in statistics and change controls A well-established Mexican pharmaceutical group with over 46 years in the pharmaceutical market We seek your talent as: **DOCUMENTATION ANALYST** **Requirements:** * Education: Degree holder in Pharmacy and Biochemistry (QFB), Pharmaceutical Chemistry (QBP), Biomedical Engineering (IBI), Food Engineering (IF), or related field. * Experience: Minimum 1 year as a documentation analyst chemist in the pharmaceutical industry. * Knowledge of GPD, GMP, GLP, GCP, NOM-059, etc. * Minimum 1 year of experience in handling and controlling documentation as required by current regulations, and in managing product dossiers. * **Mandatory proficiency in statistics and change controls related to modifications of any documentation associated with manufactured products.** * Analytical and synthesis skills, ability to deliver timely and effective solutions. * 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, food vouchers, and subsidized cafeteria service Work schedule: Monday to Friday, 9:00 AM to 6:00 PM Work location: Poniente 150 Vallejo