PROCESS SUPERVISOR

Description

Job Summary: Supervise the proper manufacturing of products by applying quality, manufacturing, productivity, and safety standards. Key Highlights: 1. Ensure alignment of procedures with regulatory requirements. 2. Train and qualify personnel under supervision. 3. Lead deviation investigations and support audits. **Date:** Apr 29, 2026 **Address:** TLAJOMULCO DE ZUÑIGA, JALISCO, MX **Company:** Grupo PiSA Live your purpose and make a difference with Grupo PiSA. With over 80 years of history, Grupo PiSA is a 100% Mexican company committed to the health and well-being of millions of people, both in Mexico and internationally. Our growth reflects the effort, passion, and dedication of a team focused on excellence. Join us and become part of a company where every day is an opportunity to live "A Life in Service of Life." Together, we can transform the future of healthcare and leave a positive impact on the world! **Employee Type** Confidence **Job Objective** Supervise the proper manufacturing of products by applying applicable quality, manufacturing, productivity, and safety standards. **Responsibilities and Activities** * Ensure that locally developed operating procedures under your responsibility are aligned with regulatory requirements. * Train and qualify personnel under your supervision in their assigned tasks according to the assigned training matrix and prior to performing their duties. * Comply with current sanitary regulations, Good Manufacturing Practices (GMP), corporate policies and directives, as well as standardized operating procedures (SOPs). * Proactively identify, review, and remain informed of changes and updates to Good Manufacturing Practice requirements. * Timely report adverse events and quality issues detected through activities under your supervision to the Quality Unit. * Maintain integrity of information and data generated across the entire documentation chain related to your responsibilities. * Lead deviation investigations assigned to your area of responsibility, providing recommendations to facilitate decision-making regarding the quality status of materials and/or products. * Support corporate audits and regulatory inspections conducted in your areas of responsibility. * Identify all areas involved in the manufacturing process with appropriate identification. * Perform cleaning activities before, during, and in auxiliary areas. * Verify process startup for approval or rejection of process initiation. * Verify that raw materials, packaging materials, labeling materials, and in-process products match identity and quantity as specified in the Production and Packaging Instructions. * Review that all manufacturing and packaging orders include necessary activities for stage-by-stage yield calculation and material reconciliation. * Supervise that all areas remain clean, orderly, and compliant with Good Manufacturing Practices. Experience * Manufacturing processes * Personnel management Knowledge * Regulatory requirements (NOM-059). * Good Manufacturing Practices * Good Documentation Practices Education Bachelor's Degree in Chemical Engineering **Complementary Profile** * Desired experience in personnel management * Flexible working hours At Grupo PiSA, we prohibit violence and discrimination, promoting equal opportunity, inclusion, and diversity. Our selection processes are FREE OF CHARGE; please report any irregularities to lineaeticagrupopisa@letica.email