Quality Supervisor

Ormco; Mexicali; Presencial; MXN 380.000 - 480.000; Jornada completa

Descripción de la vacante

Ormco in Mexicali seeks a Quality Supervisor to coordinate a team of quality inspectors and assistants, ensuring compliance with ISO 13485 and GMP requirements. You will drive continuous improvements, manage shift staffing, and communicate with other departments to ensure timely information flow.

The role requires a degree in Industrial or Mechanical Engineering, internal auditor training (desirable), and good English (60% or higher).

Formación

• Professional, preferably Industrial or Mechanical Engineer.
• Knowledge of Quality System, ISO 13485 Standards.
• Desirable experience in medical processes, molding, and/or electronics.
• Internal auditor training (desirable).
• Desirable communication in English at least 60%.
• Service attitude.
• Skills to work with staff in charge and teamwork.

Responsabilidades

• Coordinates the activities of quality inspectors, receipt inspectors, and quality assistants to ensure adherence to standards and procedures.
• Carries out improvement projects and follows up on administrative tasks.
• Defines, implements, and clarifies inspection methods; analyzes defects and disposition.
• Implements corrective and preventive actions and files rejections and documents.
• Prepares reports and manages staff scheduling, payroll verification with HR, and equipment provisioning.

Conocimientos

Quality systems

ISO 13485

English communication

Teamwork

Educación

Bachelor's degree in Industrial or Mechanical Engineering

Descripción del empleo

Summary

Coordinates the activities of a group of quality inspectors, receipt inspectors, and quality assistants, ensuring they perform their activities within the indicated standards and procedures. Additionally, carries out improvement projects in the area, follows up on administrative activities, and communicates with other departments inside and outside the company to receive and send various information as required.

Specific Job Description

QUALITY SYSTEM

• Generates and updates department procedures.
• Ensures compliance with current department procedures.
• Generates and updates controlled formats.
• Ensures compliance with good manufacturing practices in the area.
• Ensures compliance with company regulations in the supervised areas.

INSPECTION PROCESS

• Defines, implements, improves, and clarifies inspection methods.
• Analyzes the causes of defects reported by inspectors and defines disposition.
• Makes decisions on non-conforming and rejected products and materials under an MRDR (Rejection Form) and determines the applicable final disposition.
• Implements corrective and preventive actions as required.
• Files rejections and other applicable documents.

SUPERVISION

• Prepares and timely distributes various reports (production rejections [weekly], rejections and receipts [monthly], GMPs [monthly]).
• Meets weekly with quality inspectors to inform.
• Informs and provides feedback to inspectors on rejections and customer complaints.
• Verifies and confirms staff payroll with HR.
• Manages shift, schedule, and/or area movements of the staff in charge.
• Manages vacations, permits, and vacations of the staff in charge.
• Provides the necessary equipment for associates to perform their daily activities.
• Resolves different problems of the associates in charge.
• Purchases necessary equipment and tools for the quality inspector’s operation and the position itself.
• Periodically evaluates staff.
• Evaluates and strengthens staff training needs with different strategies.

Job Requirements

• Professional, preferably Industrial or Mechanical Engineer.
• Knowledge of Quality System, ISO 13485 Standards.
• Desirable experience in medical processes, molding, and/or electronics.
• Internal auditor training (desirable).
• Desirable communication in English at least 60%.
• Service attitude.
• Skills to work with staff in charge and teamwork.

Operating company:Ormco