Production Supervisor

Description

Position Summary: We are seeking a professional to supervise pharmaceutical production, ensure regulatory compliance, develop procedures, and train staff. Key Responsibilities: 1. Pharmaceutical production supervision under NOM-059-SSA1 2. Development and updating of standard operating procedures 3. Staff training on equipment usage and good practices Description and details of duties * Supervise that products are manufactured in accordance with current Good Manufacturing Practices (NOM\-059\-SSA1). * Develop and disseminate standardized operating procedures for the Production and Primary Packaging areas to ensure they remain current. * Verify correct equipment usage and maintain equipment in good condition, reporting any failures or anomalies to the Maintenance Department for review and repair. * Train and qualify staff on correct production equipment usage and area care to ensure proper execution of activities. * Ensure manufacturing records contain all required information in compliance with Good Manufacturing Practices. * Maintain yields of various processes at acceptable levels, and verify correct use of materials to reduce losses, thereby enabling continuous and efficient improvement of production processes. * Monitor and ensure compliance with manufacturing schedules. * Verify adherence to residence times of different products according to their production stage. * Pursue continuous improvement to enhance efficiency in packaging processes. * Comply with internal programs related to equipment maintenance, instrument calibration, facilities, staff training, environmental monitoring, and those required for compliance with Good Manufacturing Practices. Experience and Requirements * Bachelor’s degree in Pharmaceutical Chemistry and Biology, Chemical Engineering, Industrial Chemistry, Biochemical Engineering, or a related field in Chemical Sciences. * Minimum 3 years’ experience in a similar role within the pharmaceutical industry. * Knowledge of current NOM\-059\-SSA1. * Good Manufacturing Practices for Medicinal Products. * Knowledge of processes related to powder granulation, mixing, tablets, and hard gelatin capsules. * Personnel and material management. * Position located in TECATE, B.C. Benefits * Benefits as stipulated by the Federal Labor Law (LFT) **Number of vacancies** 1 **Department** Production/Manufacturing **Employment type** Permanent **Work modality** On-site **Shift** Day shift **Working hours** Full-time **Schedule*** Full-time **Education** Professional degree **Willingness to travel** No