Position Purpose: Supervise the adherence to good manufacturing and documentation practices, verify and analyze inputs, packaging materials, in-process products, and finished products (PT) to ensure they are manufactured according to internal specifications and comply with applicable quality and safety standards. Activities: * Clearing production lines * Verify that the area, furniture, equipment, materials, and documentation are in optimal conditions for manufacturing. * Check that personnel in the areas are free from illnesses, open wounds, long nails, are clean, without makeup or accessories, etc. * Verify that the material issued corresponds to the work order * Verify that instruments are clean, calibrated, and within validity period * Verify that the work order and all documentation are signed and reviewed by the appropriate personnel * Verify that personnel properly wear uniforms, clean clothing, hands, and nails * Record temperature and environmental conditions (relative humidity and pressure) * Verify proper completion of required documentation * Process verification * Finished products (conditioned) * Quarantine and packaging area * Inspection and analysis of inputs * Execution of analyses * Generation of results reports * Identify materials according to their assessment * Record entries in logs * Schedule analyses according to the time specified in the specification/methodology for each product and subassembly * Preparation of materials and equipment for analysis execution Number of vacancies: 2 Work modality: On-site Contract type: Indefinite Annual compensation: 13,000 **Social or economic benefits** Statutory benefits Savings fund Grocery vouchers 20 days year-end bonus Birthday day off "**Requirements** 1. Experience: 1 year in a similar position. 2. Education: High school diploma, Chemical Technician in Pharmaceuticals, Pharmaceutical Chemist-Biologist, or Chemical Engineer. 3. Specific technical knowledge. Technical-practical foundations in Quality Systems, application of physical and functional tests, evaluation of inputs and finished products, handling of laboratory equipment and measuring devices, knowledge of ANSI/ASQ Z1.4 and ANSI/ASQ Z1.9 sampling tables, sampling levels, process inspection, validation. Knowledge and familiarity with regulations on good manufacturing practices (NOM-059-SSA1, NOM-241-SSA1) and the Mexican Pharmacopoeia and Medical Devices Supplement FEUM. 4. Languages: Basic English (desirable). IMPORTANT: Work schedule: Rotating shifts: Morning shift: Monday to Saturday from 06:00 to 14:00; Evening shift: Monday to Friday from 13:45 to 21:30, Saturday from 13:45 to 20:00; Mixed shift: 08:00 to 18:00 hours. Minimum education level Bachelor's degree Languages English, intermediate level. Minimum experience 1 year Travel availability None