Quality Supervisor - 3rd shift

Sonova; Mexicali; Presencial; MXN 916,000 - 1,283,000; Jornada completa

Descripción de la vacante

A medical device company in Mexicali is seeking a Quality Supervisor for the 3rd shift. The role includes overseeing quality personnel, supporting continuous improvement initiatives, and ensuring compliance with regulatory standards. Candidates should have a Bachelor’s Degree in Engineering, at least 2 years of experience in medical device manufacturing, and strong communication skills. Proficiency in English and Microsoft Office tools is required. This position offers a chance to contribute to product quality in a high-performance environment.

Formación

• Minimum 2 years of relevant experience in a medical device manufacturing environment.
• Experience with product and procedure training, ISO standards, and Quality Systems (preferred).

Responsabilidades

• Coordinate and supervise inspection activities based on production priorities.
• Support and schedule inspections and special testing required for product release.
• Communicate personnel, process, material, and compliance issues to the QC Manager.
• Lead and coordinate inventory inspections for non-conforming components.
• Investigate corrective action requests (CARs) and drive root cause analysis.
• Review and ensure proper completion of all required quality records.
• Ensure product and process compliance with internal procedures and standards.
• Provide ongoing training and development to quality inspectors.
• Support ISO and quality system activities, aligning with regulatory requirements.

Conocimientos

Strong verbal and written communication skills

Excellent interpersonal and teamwork abilities

English proficiency: 80% or higher

Educación

Bachelor’s Degree in Engineering

Herramientas

Microsoft Word

Microsoft Excel

Microsoft Outlook

Descripción del empleo

The Quality Supervisor – 3rd Shift will be responsible for overseeing quality personnel, processes, and compliance within an assigned production area. The ideal candidate will support continuous improvement initiatives, drive adherence to quality standards, and provide strong leadership through coaching, goal-setting, and effective communication. This role plays a key part in ensuring product quality and regulatory compliance in a high-performance medical device environment.

Key Responsibilities

• Coordinate and supervise inspection activities based on production priorities, resource availability, and inspector training levels.
• Support and schedule inspections and special testing required for product release, validation builds, or non-conforming materials.
• Communicate personnel, process, material, and compliance issues to the QC Manager in a timely manner.
• Lead and coordinate inventory inspections for non-conforming components that may impact compliance with product specifications.
• Investigate corrective action requests (CARs) and drive root cause analysis, identification of solutions, and implementation of corrective actions.
• Review and ensure proper completion of all required quality records and documentation for product and process inspections.
• Ensure product and process compliance with internal procedures, industry standards, and customer quality requirements.
• Provide ongoing training and development to quality inspectors regarding procedures, standards, and quality expectations.
• Support ISO and quality system activities, maintaining alignment with regulatory requirements.

Requirements

• Bachelor’s Degree in Engineering.
• Minimum 2 years of relevant experience in a medical device manufacturing environment.
• Strong verbal and written communication skills.
• Excellent interpersonal and teamwork abilities.
• English proficiency: 80% or higher.
• Proficient in Microsoft Word, Excel, and Outlook.
• Experience with product and procedure training, ISO standards, and Quality Systems (preferred).