PROCESS SUPERVISOR

Description

Job Summary: Grupo PiSA is seeking a professional to manage material and human resources, ensuring control over documentation, labor, machinery, and raw materials in the production of solutions, in compliance with quality and safety standards. Key Highlights: 1. Committed to the health and well-being of millions of people 2. Part of a 100% Mexican company with an 80-year history 3. An opportunity to transform the future of healthcare **Date:** Apr 20, 2026 **Address:** Carr. a San Isidro Mazatepec 7, 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 mark on the world! **Employee Type** Confidential **Job Objective** Manage material and human resources to ensure control over documentation, labor, machinery, raw materials, and other materials, in compliance with applicable quality, manufacturing, productivity, and safety standards for solutions. **Responsibilities and Activities** * Coordinate and execute the production and packaging processes in accordance with the quality management system and regulatory requirements set forth by national and international authorities. * Verify that raw materials, packaging materials, packaging components, and in-process products match the identity and quantities specified in the Production and Packaging Instructions. * Ensure that all manufacturing and packaging orders include the necessary activities for calculating stage-by-stage yields and material reconciliation. * Supervise that all manufactured products are produced strictly according to authorized manufacturing instructions, adhering to the production schedule and making necessary decisions to maintain line efficiency, considering production, packaging, validation, and maintenance schedules. * Lead Quality System-related activities under a code of compliance with Good Manufacturing Practices (GMP). * Ensure that locally developed operating procedures under their responsibility align with applicable regulatory requirements (COFEPRIS, FDA, INVIMA, Canada, ISO 9001\), as well as Corporate Policies and Directives related to GMP, and remain current throughout operations. * Ensure compliance with current sanitary regulations, Good Manufacturing Practices, Corporate Policies and Directives, as well as Standard Operating Procedures (SOPs). * Perform personnel management-related activities. * Ensure implementation of the onboarding and job-specific training process for newly hired personnel. * Validate and approve any administrative requests from personnel under their supervision (e.g., work tools, incident follow-up, special leave, administrative procedures, etc.) Experience 3 years of experience in: * Pharmaceutical industries and processes. * Personnel management. Knowledge * NOM\-059 (Good Manufacturing Practices, Good Documentation Practices). * Behavior in clean areas Education Bachelor's degree in Chemical-Pharmaceutical or Chemical-Biological fields **Additional Profile** * Desired experience in personnel management. Experience Certifications Language At Grupo PiSA, we prohibit violence and discrimination, promoting equal opportunities, inclusion, and diversity. Our selection processes are FREE OF CHARGE; please report any irregularities to lineaeticagrupopisa@letica.email