TECHNICAL SUPPORT CHEMIST

Description

Position Summary: Provides technical and logistical support to the quality control laboratory, ensuring resource availability and coordination of analytical files to comply with regulatory requirements. Key Highlights: 1. Collaborate on activities related to the Quality System under GMP. 2. Coordinate the acquisition and maintenance of analytical equipment. 3. Conduct applicability testing, verification, and validation of methods. **Date:** Apr 27, 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 health and leave a positive impact on the world! **Employee Type** Confidence **Position Objective** Provide support to the quality control laboratory areas so that personnel have access to the necessary reagents, standards, supplies, instruments, and analytical equipment for raw material, intermediate product, and finished product analysis; participate in verification, validation, transfer, and development activities of analytical methods; and coordinate the analytical file for timely delivery to the Compliance Department, thereby fulfilling the manufacturing program and complying with Grupo PiSA policies and directives as well as current sanitary regulations. **Responsibilities and Activities** * Collaborate on activities associated with the Quality System under a GMP compliance code. * Coordinate the acquisition, installation, qualification, commissioning, scheduling of maintenance, verification and/or calibration of analytical equipment and instruments used in plant laboratories. * Coordinate training and certification activities for newly hired personnel. * Supervise sample receipt, reconciliation, and analytical file delivery activities. * Supervise laboratory supply control activities. * Perform applicability testing, verification, validation, and transfer of analytical and cleaning methods. Experience * Physicochemical analytical techniques – 2 years * ERP system (SAP) usage – 2 years * Procedure development – 2 years. Knowledge * Good Laboratory Practices, documentation, and manufacturing practices * Pharmacopoeias (FEUM, USP, BP) * Pharmaceutical regulations (NOM-059) * Root cause analysis tools, CAPA system, and Quality Management System. Education Bachelor's Degree **Complementary Profile** * Desired experience in deviation management and change controls, and statistical software usage. * Desired knowledge of equipment qualification, method validation and verification, and statistical analysis. Experience Certifications Language At Grupo PiSA, we prohibit violence and discrimination, promoting equal opportunities, inclusion, and diversity. Our selection processes are FREE; report any irregularity to lineaeticagrupopisa@letica.email