Quality Manager

Thermo Fisher Scientific (Planta Tijuana); Tijuana; Presencial; MXN 900.000 - 1.300.000; Jornada completa

Descripción de la vacante

The Quality Manager at Thermo Fisher Scientific Planta Tijuana leads the on-site Quality team, ensuring the effectiveness of the QMS and supporting manufacturing operations with hands-on quality leadership.

They work with Operations, Engineering, and Supply Chain to identify and resolve quality issues, drive continuous improvement, achieve KPIs, and ensure products meet customer and regulatory requirements.

Responsabilidades

• Lead and maintain site Quality System processes in line with regulatory requirements and company policies.
• Oversee CAPA, complaints, nonconformances, deviations, and change control.
• Ensure QMS records are investigated, risk-assessed, and completed on time.

Descripción del empleo

Position Summary

The Quality Manager is an on-site leadership role responsible for ensuring the effectiveness of the site's Quality Management System (QMS) while providing strong, hands-on Quality support to manufacturing operations. This position leads the site Quality team and is accountable for maintaining compliance, driving Quality performance, and fostering a culture of continuous improvement and Quality ownership throughout the organization.

The Quality Manager provides leadership and oversight for key Quality System activities, including audits, Corrective and Preventive Actions (CAPA), complaints, nonconformances, and related Quality processes, while ensuring that the Quality organization is actively engaged on the manufacturing floor.

Working closely with Operations, Engineering, Supply Chain, and other site functions, the Quality Manager and their team will identify and resolve Quality issues, improve manufacturing performance, achieve Quality KPIs, reduce recurring problems, and strengthen processes that consistently deliver products meeting customer and regulatory requirements.

Key Responsibilities

Quality Management System

• Lead and maintain effective site Quality System processes in accordance with applicable regulatory requirements, industry standards, and company policies and procedures.
• Provide oversight and governance for CAPA, complaints, nonconformances, deviations, change control, and other applicable Quality System processes.
• Ensure Quality System records are appropriately investigated, documented, risk-assessed, and completed within established timelines.