QUALITY ENGINEER

Description

Job Summary: This position ensures that finished products comply with Good Manufacturing Practices (GMP) regulatory and compliance requirements, manages the quality system, and participates in audits. Key Highlights: 1. Commitment to health and well-being, focused on excellence. 2. Ensure regulatory and compliance requirements are met for finished products. 3. Actively participate in internal and external audits. **Date:** Apr 28, 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 **Job Objective** Ensure that finished products meet regulatory and compliance requirements of Good Manufacturing Practices. **Responsibilities and Activities** * Conduct activities associated with the Quality System under a code of compliance with Good Manufacturing Practices (GMP). * Coordinate and participate in the execution of the Annual Product Review (APR), communicate results, and manage improvement opportunities. * Coordinate and execute quality release decisions for raw materials, packaging materials, and finished products. * Develop, review, and manage the Site Master File, Maquila Notices, and Technical Quality Agreements. Ensure information remains up-to-date and accessible 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. Actively participate in product market withdrawal processes, whether during simulations or actual events. Review, approve, and retain master documents and specifications. Maintain manufacturing records, analytical records, and raw material records. Experience Pharmaceutical industry Knowledge NOM 059, NOM 072 Education Bachelor's Degree in Pharmaceutical Chemistry and Biology **Complementary Profile** Willingness to work rotating shifts At Grupo PiSA, we prohibit violence and discrimination, promoting equal opportunity, inclusion, and diversity. Our selection processes are FREE OF CHARGE; report any irregularity to lineaeticagrupopisa@letica.email