Quality Systems Engineer (FMEA)

Robert Bosch Group; Guanajuato; Presencial; MXN 420.000 - 600.000; Jornada completa

Descripción de la vacante

Robert Bosch Group in Celaya, Mexico seeks a Quality Systems professional to ensure IATF 16949/ISO 9001 compliance and continuous improvement. You will implement Core Tools, support audits, manage documentation, and train staff in the quality management system.

Responsibilities include PFMEA/control plan moderation, action follow‑up, and coordination of internal audits. You will drive standardization and regulatory alignment across the plant.

Formación

• Plan, prepare, update, control, and publish Quality System documentation.
• Generate reports on the different indicators in the area.
• Audit processes and provide support in audits defined in the quality system.
• Ensure the implementation and compliance with IATF16949, ISO9001 and customer requirements.
• Manage documentation related to the quality system.
• Lead initiatives to improve processes and documentation.
• Communicate policies, standards and procedures to staff.
• Maintain regulations aligned with operations.

Responsabilidades

• Manage the internal audit program in CeaP and close IATF nonconformities.
• Coordinate Management Review (BVS-Q) and QRM with supervisor support.
• Prepare and present quality reviews and track open items to closure.
• Train CeaP staff on the quality management system.

Conocimientos

Quality Systems

Audits

Documentation

Training

PFMEA

Control Plan

Quality Improvement

IATF16949

Herramientas

IQ-RM system

BVS-Q

QRM

Descripción del empleo

Job Description

Ensure compliance and continuous improvement of the Bosch Quality System (IATF 16949/ISO 9001) through the implementation of Core Tools, internal/external audits (VDA 6.3/IATF), document management, and training, ensuring effective closure of nonconformities and the strategic deployment of the quality policy across Celaya Plant

Qualifications

As Quality Systems:

• Plan, prepare, update, control, and publish Quality System documentation
• Participate in the generation of reports on the different indicators in the area

• Audit processes and provide support in audits defined in the quality system.
• Ensure the implementation and ensure compliance with IATF16949, ISO9001 standards, customer requirements, the Bosch system, and stakeholders.
• Manage document processes related to the quality system.
• Lead initiatives to improve processes and documentation.
• Communicate policies, standards, and administrative and operational instructions to staff.
• Help users with questions about procedures, instructions, and manuals.
• Maintain current regulations in line with operational reality.
• Carry out training for CeaP employees in the quality management system, ensuring that the information is in line with current requirements
• Act as an expert on special internal and customer characteristic

As AMEF moderator and control plan:

• Confirm the PFMEA and control plan (line walks, Stand@Station, etc.).
• Ensure the implementation of the recommended actions process. Monitor, supervise, elevate, etc. the actions defined in the PFMEA.
• Define methods, standardize practices and processes at the CeaP plant.
• Moderate the PFMEA and control plan for new projects and mass production, in accordance with the established methodology and deadlines.

• Ensure the correct implementation of the FMEA process methodology by coordinating those responsible for the different manufacturing areas and complying with the CDQ0305 requirements at CeaP and specific customer requirements.
• Standardize PFMEA at CeaP (together with those responsible).
• Provide the areas involved with the necessary tools to carry out the annual update of the PFMEA in the IQ-RM system.
• Knowledge and support in documentation and review of PFMEA and Control Plan.

• Manage the internal audit program in CeaP, ensuring effective closure of IATF nonconformities and continuous improvement of the quality system.
• Coordinate and prepare the presentation for the Management Review (BVS-Q) with support from the immediate supervisor, as well as the Quality Review Meeting (QRM), and follow up on open items to ensure their effective closure.