Documentation Analyst

Description

Position Summary: We are seeking a Documentation Analyst to join a well-established pharmaceutical group focused on the management, control, and verification of documentation within the industry. Key Highlights: 1. Essential role in managing and controlling current regulatory documentation 2. Verification of correct and traceable documentation 3. Tracking of results and compliance with quality standards A strong Mexican pharmaceutical group with over 46 years in the pharmaceutical market · We seek your talent as: DOCUMENTATION ANALYST · Requirements: Education: Graduate in Pharmacy (QBP), Biochemistry (QFB), Biotechnology (IBI), Food Engineering (IF), or related field. Experience: Minimum 1 year as a chemical documentation analyst in the pharmaceutical industry. Knowledge of GMP, GLP, GDP, GCP, NOM-059, etc. Minimum 1 year experience in handling and controlling documentation required by current regulations and managing product files. 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 correct and traceable. · We Offer: ° Gross Monthly Salary ° Excellent benefits including savings fund, food vouchers, and subsidized cafeteria service Working hours: Monday to Friday, 9:00 am to 6:00 pm Work location: Poniente 150, Vallejo. -Requirements- Minimum education: Higher education – Bachelor's degree 2 years of experience Age: between 25 and 45 years Keywords: analyst