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VP, Global Quality & Regulatory Excellence

Baxter · Deerfield, IL

Apply on Baxter ↗
Level
Director+
Team
Lean / CI
Base pay
$288k–$396k
Degree
Required
Experience asked
18+ years
Industry
Medical devices
Posted
Today

The role in 30 seconds

A director-level continuous improvement role at Baxter (medical devices) in Deerfield, IL. Here, you will find more than just a job—you will find purpose and pride.

They ask for
18+ years · degree required
Tools it names
FDA / GMP, Automation
Base pay
$288k–$396k

Read from the posting. The full description is below.

From the plant jobs report · week of October 26, 2026

Continuous Improvement roles in Illinois: typical posted base $120k–$171k. This one lists $288k–$396k.

Median of the low and high ends of 14 live postings that list pay, out of 18 continuous improvement openings in Illinois, read from manufacturers' own careers sites.

Illinois plant jobs report →Pay by team and state →What moves pay →

How this role compares

Against 17 other live lean / ci postings in Illinois.

Base pay
About 149% above similar roles

Typical $113k–$162k, from 9 postings that list pay.

Experience asked
More than usual (18+ vs 10+)

Similar roles usually ask 10+ years.

Skills these teams ask for most

  • Lean 89%
  • Six Sigma 67%
  • Kaizen 61%
  • Root cause 56%
  • Black Belt 44%
  • Value stream mapping 39%

✓ = this posting asks for it too. % = share of similar postings that mention it.

It asks for 18+ years. If you're close, apply anyway: requirements are a wish list. Talk to someone doing this work there first.

At a glance

Pulled from the posting text. If it's not listed here, the posting didn't say.

How to get in at this plant

Five moves over a week or two. The first one takes ten minutes.

  1. 1

    Pick 2–3 people on the Lean / CI team at Baxter

    We found 1 person at this company and state: 1 leaders. Engineers who joined in the last year or two reply the most. See them ↓

  2. 2

    Send a short, curious note

    One real question about their work. No favors yet. Each person gets a different note, written for this role.

    Write to Lisa → (free)
  3. 3

    Turn a reply into a short call

    Questions worth asking about this team:

    • What does a normal week look like on your team?
    • Is CI run from the plant floor or from a corporate OpEx group?
    • Which metrics does leadership actually watch: OEE, scrap, cost per unit?
    • How did you land the job? What stood out in your interviews?
  4. 4

    Apply with someone vouching for you

    If the call went well, ask whether they’d pass your résumé to the hiring manager. Send your résumé link, apply that day, and let them know.

  5. 5

    Bring proof to the interview

    One page of before-and-after numbers from projects you led: scrap, OEE, cycle time, cost. Plant managers hire on results.

This plant: Baxter in Deerfield

2 other open roles at this site · 1 person we found in lean / ci roles at Baxter.

Full description from BaxterAs posted on their careers site.Show

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.

Your impact will extend across Baxter’s businesses, manufacturing network and global quality systems. You will guide enterprise priorities, investments and transformation initiatives while building scalable capabilities that improve performance and strengthen regulatory confidence.

Success will be reflected in early identification of risk, stronger operational and process performance, disciplined investment decisions, effective governance, responsible innovation, and quality capabilities built to deliver lasting business and patient impact.

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 i
Show full description ↓

This is where your 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.

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.

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