VP, Global Quality & Regulatory Excellence

Regulatory Toolkit; Deerfield (IL); On-site; USD 288,000 - 396,000; Full time

Benefits offered by this job

Medical benefits

Dental coverage

401(k) plan

Job summary

Baxter is seeking a Vice President, Global Quality & Regulatory Excellence, based in Deerfield, IL, to shape risk-aware, data-driven quality strategies across the enterprise. You will align regulatory expectations with business objectives, lead transformation programs, and drive improvements in product quality and availability while ensuring governance and human oversight.

The role requires deep regulatory engagement, cross-functional leadership, and the ability to translate external

Qualifications

• Executive experience in quality, regulatory or risk leadership.
• Experience interfacing with FDA and global health authorities.
• Ability to translate regulatory and business trends into decisions.

Responsibilities

• Shape multi-year strategy for quality excellence, regulatory resilience, and risk.
• Strengthen operations across sites and product platforms for quality.
• Lead enterprise quality transformation and scalable AI-capable initiatives.
• Guide governance for data analytics and responsible AI within quality.

Education

Bachelor’s degree (engineering / life sciences / related)

Job description

This is whereyour work makes a difference.

At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.

Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.

Here, you will find more than just a job—you will find purpose and pride.

At Baxter, the quality of our products and the strength of our regulatory practices directly support the patients and clinicians who rely on us. As Vice President, Global Quality & Regulatory Excellence, you will shape how Baxter anticipates risk, strengthens operational performance, and uses data, technology and innovation to advance quality worldwide. Based in Deerfield, Illinois, you will influence enterprise strategy and help build the capabilities that will define Baxter’s future.

Your Role at Baxter

You will lead the strategy connecting quality excellence, operational quality, regulatory resilience, enterprise risk, data and analytics, and responsible artificial intelligence. Working closely with the senior Quality leadership team and leaders across Baxter, you will translate emerging regulatory, technology and business trends into decisions that protect patients, strengthen product availability and quality, and support sustainable growth.

What You'll Be Doing

• Shape Baxter’s multi-year strategy for quality excellence, operational quality, regulatory resilience, enterprise risk, data, analytics and responsible AI, aligning priorities with patient needs and business strategy.
• Strengthen operational quality across manufacturing sites, product platforms, supply networks and quality systems by identifying systemic opportunities and driving improvements in reliability, compliance and product availability.
• Lead enterprise quality transformation and targeted interventions, focusing expertise and investment where they can create the greatest patient, regulatory and business value and scaling successful approaches across Baxter.
• Advance Baxter’s digital quality and analytics strategy by prioritizing scalable technology, automation and AI capabilities that improve insight, decision-making and organizational performance while maintaining appropriate governance and human oversight.
• Anticipate changes in U.S. Food and Drug Administration (FDA) and global health authority expectations, translating external developments into proactive regulatory strategies, preparedness priorities and enterprise decisions.
• Guide enterprise risk, operating-plan and capital-investment decisions by connecting quality and regulatory priorities with patient and product risk, resilience, financial stewardship and long-term value.
• Build a strong global leadership and talent pipeline, developing the capabilities Baxter will need across operational quality, strategic risk, data, technology and transformation while creating alignment across businesses, functions and geographies.

What You'll Bring

• Bachelor’s degree in Engineering, Life Sciences, Pharmacy, Microbiology, Chemistry, Quality, Regulatory Affairs, Data Science, Business, or a related discipline.
• At least 18 years of progressive leadership experience, including significant executive responsibility in Quality, Regulatory Affairs, Compliance, Manufacturing, Operations, Enterprise Risk, Digital Transformation, or a related discipline within medical device, pharmaceutical, healthcare, or another highly regulated industry.
• Demonstrated success at the Vice President or comparable enterprise level, setting strategy and leading transformation across a complex global organization with measurable patient, regulatory, operational, financial and organizational impact.
• Deep operational quality experience spanning manufacturing, supply chain, product lifecycle, quality systems, inspection readiness, remediation and continuous improvement, together with experience engaging the FDA and other global health authorities.
• Experience leading significant operating budgets and influencing capital investment, resource allocation, business cases and investment priorities.
• Ability to advise senior executives and communicate complex quality, regulatory, operational and risk considerations clearly to executive and Board-level audiences.
• Demonstrated success leading across organizational boundaries, building strong leadership capability and using data, analytics and external insights to improve strategic decision-making.

Preferred Qualifications

• Advanced degree such as an MBA, MS, PhD or PharmD.
• Executive education or recognized certification in enterprise risk management, data analytics, artificial intelligence, digital transformation or quality leadership.
• Experience as an enterprise Quality or Regulatory executive, Site Quality Head, senior Operations leader, or comparable global technical leader with broad business and financial accountability.
• Experience sponsoring or governing AI, machine learning, automation or digital quality initiatives, including consideration of model risk, privacy, cybersecurity, data integrity and regulatory requirements.

We understand compensation is an important factor as you consider the next step in your career. At Baxter, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated base salary for this position is $288,000 - $396,000annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based on upon location, skills and expertise, experience, and other relevant factors. This position may also be eligible for discretionary bonuses, commission, and/or long-term incentive. For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview.

US Benefits at Baxter (except for Puerto Rico)

This is where your well-being matters. Baxter offers comprehensive compensation and benefits packages for eligible roles. Our health and well-being benefits include medical and dental coverage that start on day one, as well as insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance. Financial and retirement benefits include the Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount, and the 401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching. We also offer Flexible Spending Accounts, educational assistance programs, and time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave. Additional benefits include commuting benefits, the Employee Discount Program, the Employee Assistance Program (EAP), and childcare benefits. Join us and enjoy the competitive compensation and benefits we offer to our employees.For additional information regarding Baxter US Benefits, please speak with your recruiter or visit our Benefits site: Benefits | Baxter

Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time.

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.

Know Your Rights: Workplace Discrimination is Illegal

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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