Position Summary: This position ensures that finished products comply with regulatory and Good Manufacturing Practice (GMP) requirements, by participating in audits and managing quality documentation. Key Highlights: 1. Ensure regulatory compliance in pharmaceutical product manufacturing. 2. Develop and manage key quality and regulatory documentation. 3. Actively participate in internal and regulatory audits. **Date:** Feb. 18, 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!**Type of Collaborator** Confidence**Position Objective** Ensure that finished products comply with regulatory and Good Manufacturing Practice (GMP) requirements. **Responsibilities and Activities** * Ensure that operating procedures and local documents developed 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 valid throughout operations. * Comply with current sanitary regulations, Good Manufacturing Practices, Corporate Policies and Directives, as well as Standard Operating Procedures (SOPs). * Prepare the Annual Product Review and evaluate each established quality system, classifying findings and generating corresponding deviations. * Develop, review, and manage the Site Master File for Manufacturing, Toll Manufacturing Notices, and Technical Quality Agreements. Ensure information remains updated and available at all times. * Actively participate in Internal Audits, Customer Audits, Regulatory Audits, and Third-Party Audits. Follow up on deviations, change controls, and assigned action plans. * Review, approve, and safeguard master documents and specifications. Maintain manufacturing records, analytical records for manufacturing, and raw material records. Experience * 1 year in the pharmaceutical industry Knowledge NOM 059, NOM 072 Education Bachelor’s degree in Chemistry or Chemical Pharmacy and Biology**Complementary Profile** * Quality, Development, Research or Laboratory areas * Research Centers 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