Overview
This is where you make a difference in our patients’ safety. As a member of the Baxter Quality team, you will play an essential part in our mission of saving and sustaining lives. Quality is important throughout the entire product lifecycle and works collaboratively with all areas of the organization. Because Quality touches everything Baxter does, a role in Quality provides many opportunities for growth, learning and a successful career that has a daily impact on people’s lives.
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Support for Parents
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Continuing Education/
Professional Development -
Employee Health &
Well-Being Benefits -
Paid Time Off
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2 Days a Year to Volunteer
Success Profile
What makes a successful Quality team member at Baxter? Take a look at some of the top traits we’re looking for and see if you’re a fit.
- Detail Oriented
- Continuous Learner
- Courageous
- Collaborative
- Critical Thinker
- Influential
Supplier Quality Engineer
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.
Summary
Working as Supplier Quality Engineer is the way to be an active stakeholder in Supplier Evaluation and Supplier Auditing process. You’ll collaborate closely with other departments as R&D, Manufacturing, QA Operations and Purchasing in order to ensure that purchased products and/or services are conform to the requirements.
Essential Duties and Responsibilities
- Suppliers’ evaluation according to applicable procedures/policies;
- Perform Design Transfer to suppliers and make sure new implemented processes are capable for production;
- Define, perform and document the dispositions versus the Suppliers in case of non-conforming products;
- Evaluation and monitoring of the suppliers’ performance data in order to identify eventual corrective or improvement actions;
- Support investigations and verify the efficacy of the corrective actions implemented by suppliers;
- Support local sites inspection by providing, in a timely manner, proper suppliers’ data;
- Support proper reporting of suppliers’ performance;
Qualifications
- University degree in life science field, Engineering, Chemical or Biology;
- Preferred previous experience in Pharma/API/Medical company;
- Knowledge of Quality System requirements based on GMP regulations, FDA CFR, MDSAP and ISO13485, MDR;
- Experienced on typical product defects identified in field and in production and root cause investigation;
- Knowledge of statistical analysis;
- Fluent in English, knowledge of other languages will be considered a plus.
Reasonable Accommodations
Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please send an e-mail to [email protected] and let us know the nature of your request along with your contact information.
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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