Quality Supervisor - 2nd shift

Sonova; Mexicali; Presencial; MXN 1,104,000 - 1,474,000; Jornada completa

Descripción de la vacante

A medical device company in Mexicali is seeking a Quality Supervisor in Production to oversee inspection activities and enhance processes using lean manufacturing techniques. The ideal candidate will have a Bachelor's degree in Engineering and over two years of relevant experience in the medical device industry, along with strong communication and interpersonal skills. This role includes team building, goal setting, and ensuring compliance with quality standards.

Formación

• 2+ years of relevant experience in a medical device environment.
• Product and procedure training is required.
• ISO & Quality overview knowledge.

Responsabilidades

• Coordinate regular inspection activities for quality assurance.
• Inform QC manager about compliance concerns.
• Investigate and implement corrective actions.
• Ensure compliance with quality standards.

Conocimientos

Verbal and written communication skills

Interpersonal skills

Proficient in Microsoft Word

Proficient in Microsoft Excel

Proficient in Microsoft Outlook

English (80%)

Educación

Bachelor Degree in Engineering

Descripción del empleo

The Quality Supervisor in Production will be directly responsible for people and processes of a designated operations process area. This candidate will develop and improve processes using lean manufacturing techniques. This leader will provide team building, goal setting, and change management. Key Tasks & Responsibilities:

• Coordinates and supports regular inspection activities based on priority production and availability/training of Quality inspectors. Coordinates inspections and special tests for the release of products in validation or non-conforming.

• Inform QC manager about personnel, process, material and compliance concerns.

• Notifies and coordinates inventory inspections of non-comforting components that impact compliance with product specifications.

• Investigate corrective action requests and identify / implement solutions.

• Reviews and coordinates with leaders / inspectors the correct compliance to fill the quality records required in the inspection process to the products / processes.

• Assure that product and process quality is compliant to internal, industry and customer quality standards.

• Bachelor Degree in Engineering
• 2+ years of relevant experience in medical device environment
• Proficient verbal and written communication skills
• Excellent interpersonal skills
• English 80%
• Proficient in Microsoft Word, Excel, and Outlook
• Product and procedure training
• ISO & Quality overview