Quality Auditor

Description

Job Summary: We are seeking a Quality Auditor to identify and prevent quality/regulatory non-compliances through the management and execution of internal and supplier audits. Key Highlights: 1. Key role in preventing quality and regulatory non-compliances. 2. Participation in internal, supplier, and customer audits. 3. Opportunity to work in the medical device and pharmaceutical sector. **Job ID** R\-537510 **Date posted** 27 February 2026 **Job Description Summary** =========================== Do you want to become a creator of the possible? For over 125 years, we have pursued our purpose by advancing the world of health™. We relentlessly commit to a promising future by developing innovative technologies, services, and solutions—helping the healthcare community improve safety and increase efficiency. It takes the imagination and passion of all of us at BD—from manufacturing to marketing our products—to envision the impossible and discover transformative solutions that turn our dreams into possibilities—for people today, tomorrow, and in the future. Join us as a creator of the possible! With innovative pre-filled syringes, auto-injection systems, safety systems, and needle technologies, the Pharmaceutical Systems (PS) team offers a broad portfolio of solutions designed to protect, package, and deliver drug therapies. Quality Auditor Identify and prevent actual or potential quality and/or regulatory non-compliances or deviations through the development, management, execution, and follow-up of the internal and supplier quality audit program, as well as coordination and management of customer, corporate, health ministry, and certification body audits.**Job Description** =================== **Functions and Responsibilities:** * Conduct internal audits by developing, managing, and executing the quality system audit program, with the objective of ensuring compliance with internal and external regulations. * Conduct supplier audits by developing, managing, and executing the supplier audit program, with the objective of ensuring compliance with agreed specifications or established technical agreements. * Track and verify closure of corrective actions identified during internal, supplier, ISO certification body, health ministry, and customer audits, per current procedures. * Train users of the eAudit system and ensure effective communication with them to guarantee adherence to committed deadlines and effectiveness of corrective/preventive actions. * Serve as the point of contact with the global Supplier Audit Team (SMAT) and update information in the global supplier management system (SMIS). * Maintain up-to-date area-specific procedures and ensure compliance by involved functions. Likewise, provide necessary information for generating metrics on the audit process status. * Maintain qualification as a Supplier Auditor/Lead Auditor/Internal Auditor per guidelines outlined in applicable procedures or work instructions. **Requirements:** * Engineering or Chemical-Biological Sciences or related field. * 2–3 years of experience. * Quality audits; RCA; Regulatory Compliance in the Pharmaceutical Industry, Medical Devices, ISO 9001 or ISO 13485\. * Advanced English. * Auditor certified by an accreditation body, e.g., SQA, IRCA. (Desirable) * CAPA system proficiency. (Desirable) * Trackwise proficiency. (Desirable) *"BD values workplace equity and does not discriminate against any disability, class, ethnicity, age, religion, gender identity, or sexual orientation".* Required Skills Optional Skills . **Primary Work Location** ========================= MEX Cuautitlan Izcalli**Additional Locations** ======================== **Work Shift** ==============