Quality Engineering Supervisor – Medical Devices & CAPA

Cardinal Health; Tijuana; Presencial; MXN 600.000 - 1.200.000; Jornada completa

Descripción de la vacante

Cardinal Health is seeking a seasoned quality leader in Mexico to advance our quality system and CAPA program at a manufacturing site in TJ. The role focuses on maintaining product quality and safety for medical devices, coordinating root-cause investigations, and driving process improvements across functions.

Ideal candidates have 8+ years of experience, a related degree or equivalent work background, and strong English skills. Experience with QSR, CAPA, and validation is preferred.

Formación

• 8+ years of experience preferred.
• Advanced English is required.
• Medical industry experience preferred.
• PowerBI and AI knowledge preferred.

Responsabilidades

• Develop and implement interdepartmental and multifunctional relations to promote the quality system (QSR).
• Influence metrics of the quality system (CAPA, training, completion, complaints).
• Manage quality systems, processes, and procedures to guarantee product quality and safety.
• Lead or assist in resolving non-conformities and CAPA actions.
• Lead development of better processes and streamline existing ones.
• Collaborate to improve processes and boost efficiency.
• Manage the operations quality control team to meet goals.
• Review/approve non-conforming material and change requests.
• Provide leadership, problem solving, and coaching to team members.
• Experience in medical device manufacturing operations, including verification and validation.
• Coordinate root cause investigations with multifunctional teams.
• Follow safety rules to prevent accidents and environmental issues.
• Participate in projects to reduce plant costs.
• Responsible for validation and maintenance of test methods and equipment.

Conocimientos

Advanced English

Educación

Bachelor's degree or equivalent experience

Herramientas

PowerBI

AI knowledge

Descripción del empleo

Cardinal Health is seeking a seasoned quality leader in Mexico to advance our quality system and CAPA program at a manufacturing site in TJ. The role focuses on maintaining product quality and safety for medical devices, coordinating root-cause investigations, and driving process improvements across functions.

Ideal candidates have 8+ years of experience, a related degree or equivalent work background, and strong English skills. Experience with QSR, CAPA, and validation is preferred.