Jr Supplier Quality Engineer

Foxconn Baja California, S.A. de C.V.; Tijuana; Presencial; MXN 360.000 - 480.000; Jornada completa

Descripción de la vacante

Foxconn Baja California, S.A. de C.V. seeks a Quality/Process Engineer to support supplier evaluations, incoming material inspections, RMS reviews, and MRB management on the production floor.

The role centers on maintaining quality controls and compliance in a regulated manufacturing setting. The ideal candidate has 1–3 years in quality or production, with ISO 13485 knowledge, and can communicate in English (B1).

Formación

• Bachelor’s degree in Industrial, Quality, Biomedical Engineering, or related field.
• 1–3 years of experience in quality, processes, or production (preferably in medical or regulated industry).
• Experience on the production floor.
• Intermediate English (B1).

Responsabilidades

• Communicate and follow up on supplier evaluations and audits.
• Coordinate receipt and inspection of incoming materials against specifications.
• Follow up on raw material specifications (RMS).
• Collaborate in supplier development and continuous improvement.
• Monitor supplier performance indicators and report results.
• Manage non-conforming material (MRB), RMAs, and credit notes.
• Analyze data to anticipate risks and improve the supply chain.
• Participate in projects to optimize purchasing and quality processes.
• Maintain communication with purchasing and production teams.
• Promote a quality culture within the supply chain.
• Support process validation activities on the production floor in a medical environment (IQ, OQ, PQ).

Conocimientos

Quality management

Process improvement

Production floor experience

English (B1)

Educación

Bachelor’s degree in Industrial, Quality, Biomedical Engineering, or related field

Herramientas

ISO 13485

RMS

MRB/RMA

Traceability docs

Descripción del empleo

Main Responsibilities

1. Communicate and follow up on supplier evaluations and audits.
2. Coordinate the receipt and inspection of incoming materials, ensuring compliance with specifications.
3. Follow up on raw material specifications (RMS).
4. Collaborate in supplier development and continuous improvement.
5. Monitor supplier performance indicators and report results.
6. Manage non-conforming material (MRB), RMAs, and credit notes.
7. Analyze data to anticipate risks and improve the supply chain.
8. Participate in projects to optimize purchasing and quality processes.
9. Maintain effective communication with purchasing and production teams.
10. Promote a quality culture within the supply chain.
11. Participate on the production floor as process engineering support, ensuring compliance with specifications and quality controls.
12. Support process validation activities in a medical environment (IQ, OQ, PQ), ensuring compliance with established requirements.

Requirements

1. Bachelor’s degree in Industrial, Quality, Biomedical Engineering, or related field.
2. 1–3 years of experience in quality, processes, or production (preferably in medical or regulated industry).
3. Experience on the production floor.
4. Intermediate English (B1).

Technical Knowledge

• ISO 13485
• Raw Material Specifications (RMS)
• Non-conforming material management (MRB, RMA)
• Traceability and documentation
• Manufacturing processes on the production floor
• Process validation (IQ, OQ, PQ)