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:

Responsible for providing Quality support and may include oversight via direct staff supervision or process/area responsibilities. Identify and assess regulatory and quality risk in activities and processes according to regulatory agency rules and guidelines and Baxter quality practices.

Essential Duties and Responsibilities:

·Lead daily departmental activities for areas of direct responsibility

·Create and / or analyze operation metrics and reports to identify improvement opportunities

·Write, review, analyze and revise written Standard Operating Procedures (SOPs) and submit procedural changes as needed to meet Corporate, Divisional, Plant, Regulatory Requirements, etc

·Participate in external assessments and audits by evaluating and solving product/process problems by providing technical, analytical and supervisory skills Support process with timely closure of observations/audit items.

·         Support other site needs as assigned.

Preferred Qualifications:

·Working knowledge of medical products

·Excellent computer skills

·Knowledge of JDE

·Good communication, written and oral skills

·Knowledge of regulations outside United States a plus

·Self-motivated with the ability to work independently and make decisions

·Excellent organizational skills, problem solving skills and attention to detail

·Ability to perform multiple tasks simultaneously and work cross-functionally in a highly-matrixed environment

·Ability to drive decisions and actions

·Expertise in interpreting regulations and familiarity with GDP and GMP

·Experience with working in an environment subject to compliance with 21 CFR Parts 7, 11, 803, 806, 810, 820 strong preferred

Education and/or Experience:

• BS in business or science or equivalent 
• 1-5 years experience in Quality or technical industry

The successful candidate for this job may be required to verify that he or she has been vaccinated against COVID-19, subject to reasonable accommodations for individuals with medical conditions or religious beliefs that prevent vaccination, and in accordance with applicable law.

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.

EEO is the Law 
EEO is the law - Poster Supplement
Pay Transparency Policy

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

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