Specialist Quality Supplier

hace 2 semanas

Monterrey, México BAXTER A tiempo completo

**This is where you save and sustain lives**

At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.

Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.

Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.

Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission.

**DUTIES AND RESPONSIBILITIES**:

- Develop a transfer plan based a global quality plan for the site.
- Develops and communicates Hill-Rom’s expectations for quality performance, continuous improvement, quality systems, process controls infrastructure for high leverage/critical sustaining parts and new products sources to suppliers.
- Performs and coordinates quality system and process control assessments.
- Measures and communicates supplier performance on key metrics and the corresponding continuous improvement plans.
- Participates as an active member in the new product development process supplier evaluation team and the sourcing core team.
- Collaborates, trains and mentors supplier representatives in best practices, Iike quality systems, process controls methods, problem solving and statistical tools.
- Monitors and drives corrective action and continuous improvement activities that directly impact performance for assigned suppliers.
- Follow up supplier nonconformance material to proper disposition and implementation of actions to resolve nonconformance’s at supplier facility.
- If needed SQE will be coordinate a team of technicians to follow up supplier nonconformance’s.

**EDUCATION**
- College degree required, with preference to engineering or scientific disciplines.

**EXPERIENCE**:

- A minimum of 3-8 years’ experience in quality assurance or regulatory affairs, with medical device experience preferred.
- Practical experience in metrology, test, inspection and analysis techniques.
- Experience in the medical device industry or automotive industry in development and deployment on quality system and process controls and continuous improvement methods (QSR’s, ISO9000/QS9000, ISO13485).
- Primary/secondary compliance auditing experience.

**QUALIFICATIONS**:

- Demonstrated strong analytical, problem solving, teaming and communication/interpersonal skills.
- Computer competency in Word, Excel, Power Point and databases.
- Ability to work independently.
- Ability to methodically manage projects.
- Bilingual.

**Reasonable Accommodations**

**Recruitment Fraud Notice**

Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

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