Position Summary: We are seeking a collaborator to support the quality control laboratory, ensuring resource availability and participating in the development and validation of analytical methods to comply with the manufacturing program and health regulations. Key Highlights: 1. Critical support for the quality control laboratory. 2. Participation in validation and development of analytical methods. 3. Ensuring compliance with the manufacturing program and health regulations. **Date:** Jan. 28, 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 health and leave a positive impact on the world! **Collaborator Type** Trust-Based **Position Objective** Provide support to quality control laboratory areas so that personnel have access to necessary reagents, standards, supplies, analytical instruments, and equipment for raw material, intermediate product, and finished product testing; participate in verification, validation, transfer, and development activities of analytical and cleaning methods; as well as coordinate the analytical dossier for timely delivery to the Compliance Department, thereby fulfilling the manufacturing program and adhering to Grupo PiSA’s policies and directives, as well as current health regulations. **Responsibilities and Activities** * Collaborate in activities associated with the Quality System under a Good Manufacturing Practices (GMP) compliance code. * Coordinate acquisition, installation, qualification, registration, maintenance scheduling, verifications, and/or calibrations of analytical equipment and instruments in plant laboratories. * Coordinate training and certification activities for newly hired personnel. * Supervise sample receipt, reconciliation, and analytical dossier delivery activities. * Supervise laboratory supply control activities. * Conduct applicability testing, verification, validation, and transfer of analytical and cleaning methods. Experience 1 year in physicochemical analysis of process products, raw materials, and finished products. 1 year with laboratory instrumentation equipment (HPLC, UV, IR, Gas Chromatography). 1 year in the pharmaceutical, cosmetic, food, or related industry. Knowledge Pharmacopoeias (FEUM, USP, BP) and international standards (ICH, PDA). Standard 059 (Good Laboratory Practices, documentation, storage, etc.). Education Bachelor's Degree **Complementary Profile** Availability to rotate shifts (day/night). Adherence to Standards. Process Control. 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