Eng. Supplier Quality

Baxter Healthcare - Welch Allyn de Mexico, S. de R.L. de C.V.; Tijuana; Presencial; MXN 420.000 - 600.000; Jornada completa

Descripción de la vacante

Baxter Healthcare - Welch Allyn de Mexico, S. de R.L. de C.V. seeks a Sr Eng, Supplier Quality to plan, coordinate and execute audits worldwide, ensuring supplier quality in manufacturing processes at Baxter.

The role emphasizes problem solving, corrective action management, and collaboration with sourcing and manufacturing teams to drive supplier performance improvements.

Formación

• Degree in Engineering required.
• Knowledge of FDA CFR 820, ISO 13485 and ISO 9000 requirements; ISO 13485 Lead Auditor preferred.
• English proficiency required.
• 3+ years experience in quality/audit roles, especially supplier audits.

Responsabilidades

• Plan, coordinate and execute supplier audits domestically and internationally.
• Follow up on audits to demonstrate supplier controls.
• Develop inspection and test techniques for supplier materials.
• Lead supplier approval by assessing manufacturing and quality systems.
• Manage SCARs and ensure timely corrective actions.
• Reduce MRB inventory through problem solving with Manufacturing and Quality teams.

Conocimientos

Supplier Quality

Auditing

Problem Solving

Documentation

English

Educación

Engineering Degree

Descripción del empleo

Your role at Baxter:

This position participates in supplier quality related to monitoring and improvement of supplier performance. Coordinates problem solving from parts supplied.

Your team:

From your role as Sr Eng, Supplier Quality #This is where we count on your knowledge and talent to be responsible for planning, coordinating, scheduling and executing supplier audits nationally and internationally ensuring supplier quality in manufacturing processes at Baxter.

What you’ll be doing:

• Plan, coordinate, Schedule, execute supplier audits domestically and internationally as required.


• Follow up on supplier audits to demonstrate supplier controls required by FDA CFR 820, ISO 13485 and ISO 9000.


• Work with sourcing staff to coordinate supplier audits activities as required.


• Develops inspection and test techniques to evaluate supplier materials.


• Works with suppliers to find solutions to identified problems.


• Manage and insure timely implementation of supplier Corrective Action Reports (SCARs).


• Lead the supplier approval process by assessing manufacturing, Quality Systems capabilities and risks.


• Manages personnel maintain and reduce the Incoming Inspection cycle time.


• Establishes problem solving strategies and work with Manufacturing and Quality Engineers to reduce MRB inventory.


• Perform component characteristic analysis to determine inspection status changes.

What you’ll bring:

• Degree in Engineering required.


• Knowledge of FDA CFR 820, ISO 13485 and ISO 9000 requirements, strongly desired ISO 13485 Lead Auditor certification


• English


• Desirable experience: 3 years or more of experience.


• previous experience with quality auditing, specifically supplier audits. Excellent documentation, communication and excellent problem-solving skills are desirable.