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.

About Us: Baxter’s Mission:

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 90 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful, and encourage each other.

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

Your role at Baxter:

As Engineer II, Quality (CAPA & Complaints) your role is essential to ensuring that Baxter's Quality System Regulation requirements are met, and that the company's products and processes are of the highest quality and safety.

Your team:

We develop quality products with the patient in mind, so our efforts are also patient centric. That means you can be proud of our work and the value we provide to people every day.

As a large, multinational organization, you have the opportunity to expand your knowledge through collaboration with a variety of individuals, exposure to different facets of our portfolio, and a supportive leadership team that encourages ongoing development.

What you’ll be doing:

• Participate and maintain full knowledge of the Operations / Management Review.
• Support the design and development improvement of new product processes and technologies.
• Owner of non-conformance investigation and audits items as applicable.
• Evaluate failure modes (PFMEA) related with process, product and machines.
• Assure Good Documentation Practice (GDP) and Good Manufacturing Practice (GMP) principles are used in the process/documents handle in the areas under responsibility.
• Analyzed areas indicators and submit them to management for review and monthly Process Data Review in the corresponding quality boards to promote and strengthen the plant processes.
• Approve related local specifications, procedures and required documents.
• Develop and support continuous improvement activities to enhance the Quality Systems, using quality and continuous process improvement tools, including but not limited to Six Sigma, Kaizen lean methods, etc.
• Responsible for activities coordination of the investigators.
• Indirectly supervises the personnel for other areas, such as manufacturing, and product and process engineers assigned to analyze root causes and implement corrective and preventive actions.
• Coordinate with different areas the need to open CAPA’s due to nonconformance detected and unfavorable trends as established in the procedures.
• Standardized/ consolidate investigations of different types of process / products deviations to ensure consistency among them, accurate classification of the non-conformance, as well as to ensure that proposed actions to accurate them do not contradict actions already implemented.
• Responsible for preparing and realization of the metrics reported at periodic meetings like Product Quality Data Review (PQDR/Indicators), Management Review boards (MRB), Local and Americas CAPA Review Board (CRB) of the CAPA/ NCR systems.

What you’ll bring:

• Bachelor’s degree in science, pharmacy, industrial engineering or related field.
• 3 - 5 years of proven ability in quality or related areas.
• Experience in validation processes, manufacturing process of medical devices and implementation of projects.
• Experience in Investigations, CAPA, NCR or complaints.
• Bilingual.

Equal Employment Opportunity

Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status, or any other legally protected characteristic.

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on thelinkhere and let us know the nature of your request along with your contact information.

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here 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.