PROCESS SUPERVISOR

Description

Job Summary: Manage material and human resources, controlling documentation, labor, machinery, and raw materials to meet quality, manufacturing, productivity, and safety standards for solutions. Key Highlights: 1. Committed to the health and well-being of millions of people. 2. Be part of a company where every day is an opportunity. 3. Transform the future of healthcare and leave a positive legacy. **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 impact on the world! **Employee Type** Trust-based **Job Objective** Manage material and human resources to control documentation, labor, machinery, raw materials, and supplies, adhering to applicable quality, manufacturing, productivity, and safety standards for solutions. **Responsibilities and Activities** * Coordinate and execute production and packaging processes in compliance with the quality system and in adherence to regulatory requirements from national and international authorities. * Verify that raw materials, packaging materials, packaging components, and in-process products match identity and quantity as specified in the Production and Packaging Instructions. * Ensure that all manufacturing and packaging orders include necessary activities for calculating stage-wise yield and material reconciliation. * Supervise that all manufactured products are produced strictly per authorized manufacturing instructions, meeting the production schedule while making necessary decisions to maintain line efficiency, considering production, packaging, validation, and maintenance schedules. * Lead activities associated with the Quality System under a Good Manufacturing Practice (GMP) compliance code. * Ensure that locally developed operating procedures under your responsibility align with applicable regulatory requirements (COFEPRIS, FDA, INVIMA, Canada, ISO 9001\), as well as Corporate Policies and Directives related to GMPs, and remain current during operations. * Ensure compliance with current sanitary regulations, Good Manufacturing Practices, Corporate Policies and Directives, as well as Standard Operating Procedures (SOPs). * Perform activities related to personnel management. * Ensure execution of the onboarding and job-specific training process for newly hired personnel. * Validate and approve any administrative requests from personnel under your supervision (work tools, incident follow-up, special permissions, 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; report any irregularity to lineaeticagrupopisa@letica.email