ResponsibilitiesManage and ensure compliance with the Quality Management System under applicable standards such as ISO ****, ISO *****, and customer-specific requirements.Ensure compliance with regulations applicable to medical and electronic products.Lead internal, external, customer, and regulatory audits.Develop and implement continuous improvement strategies focused on reducing defects, rework, and cost of poor quality.Supervise Incoming Quality, IQC, IPQC, OQC, SQE, Document Control, and Supplier Quality areas.Monitor and track quality key performance indicators (KPIs).
Coordinate root cause analysis and corrective/preventive actions using tools such as 8D, CAPA, Fishbone, 5 Why's, and FMEA.Ensure proper validation and control of electronic manufacturing and special processes.Participate in New Product Introduction (NPI) transfers and engineering changes.Ensure training and development of quality department personnel.Maintain effective communication with customers regarding quality issues, complaints,



and corrective actions.Coordinate certification programs and regulatory compliance activities.Promote a culture of quality, safety, and continuous improvement within the organization.Education & ExperiencePostgraduate degree preferred.Minimum of 5 years of experience in similar roles.Advanced English proficiency (C2 level).
Experience supervising supervisors and leading teams.Direct customer interaction experience.Technical SkillsISO ****ISO *****IPC-A-610FDA / GMP (preferred)Core Tools: PFMEA, Control Plan, SPC, MSALean Manufacturing and Six SigmaCAPA and Root Cause AnalysisSMT processes and electronic assembly manufacturingInterpretation of technical specifications and documentationSoft SkillsLeadershipEffective communicationDecision-makingProblem-solvingNegotiation with customers and suppliersOrganization and follow-upAbility to work under pressure#J-*****-Ljbffr

📌 Quality Manager | Electronics - Smt | Ct (Tijuana)
🏢 Grupo TECMA
📍 Tijuana