Quality Manager | Electronics - SMT | CT

Grupo TECMA; Tijuana; Presencial; MXN 1.040.943 - 1.561.415; Jornada completa

Descripción de la vacante

Grupo TECMA in Tijuana seeks a quality management leader to oversee compliance with standards like ISO 9001 and ISO 13485. The successful candidate will lead audits, implement improvement strategies, and ensure the training of personnel in a dynamic environment.

A postgraduate degree and 5+ years of experience in similar roles are preferred. Advanced English proficiency and the ability to work under pressure are essential. Join us in promoting a culture of quality and continuous improvement!

Formación

• Minimum of 5 years of experience in similar roles.
• Experience supervising supervisors and leading teams.
• Direct customer interaction experience.

Responsabilidades

• Manage and ensure compliance with the Quality Management System under applicable standards.
• Ensure compliance with regulations applicable to medical and electronic products.
• Lead internal and external audits.
• Develop and implement continuous improvement strategies.
• Monitor and track quality key performance indicators (KPIs).
• Coordinate root cause analysis and corrective actions.

Conocimientos

Leadership

Effective communication

Decision-making

Problem-solving

Negotiation with customers and suppliers

Organization and follow-up

Ability to work under pressure

Advanced English proficiency

Educación

Postgraduate degree preferred

Herramientas

ISO 9001

ISO 13485

Lean Manufacturing

Six Sigma

CAPA

Root Cause Analysis

PFMEA

Control Plan

SPC

MSA

FDA / GMP

IPC-A-610

Descripción del empleo

Responsibilities

• Manage and ensure compliance with the Quality Management System under applicable standards such as ISO 9001, ISO 13485, 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 & Experience

• Postgraduate 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 Skills

• ISO 9001
• ISO 13485
• IPC-A-610
• FDA / GMP (preferred)
• Core Tools: PFMEA, Control Plan, SPC, MSA
• Lean Manufacturing and Six Sigma
• CAPA and Root Cause Analysis
• SMT processes and electronic assembly manufacturing
• Interpretation of technical specifications and documentation

Soft Skills

• Leadership
• Effective communication
• Decision-making
• Problem-solving
• Negotiation with customers and suppliers
• Organization and follow-up
• Ability to work under pressure