Senior Director, Quality - Medical Devices,

Baxter International Inc.; Round Lake (IL); On-site; USD 216,000 - 297,000; Full time

Benefits offered by this job

Health insurance

401(k) plan with company matching

Paid time off (20–35 days)

Employee Stock Purchase Plan (ESPP)

Job summary

Baxter International Inc. is seeking a Senior Director, Quality - Medical Devices to lead strategy and governance for quality across a global medical device network.

You will oversee Design Quality, Manufacturing Quality, and Post-Market Surveillance, partnering with executive leaders to drive lifecycle excellence and regulatory readiness. The role requires 15+ years in quality leadership within medical devices, a engineering/science degree (advanced degree preferred), and a track record of

Qualifications

• 15+ years of progressive quality leadership experience in the medical device industry.
• Bachelor's degree in Engineering, Science, or related discipline required; advanced degree preferred.
• Deep expertise in medical device quality systems, regulatory requirements, inspection management, and risk mitigation.
• Proven ability to lead Design Quality, Manufacturing Quality, and Post-Market Surveillance organizations within a regulated medical device environment.

Responsibilities

• Develop and execute a multi-year Quality strategy across Baxter's medical device network.
• Lead Quality governance and decision-making across multiple sites and functions.
• Provide executive oversight for Design Quality, Manufacturing Quality, and Post-Market Surveillance activities across the lifecycle.
• Partner with senior leaders across Manufacturing, R&D, Regulatory Affairs, Supply Chain, Finance, HR, and Commercial to support lifecycle management and reliable product supply.
• Champion regulatory compliance and inspection readiness globally.
• Ensure integration of Design Quality, Manufacturing Quality, Regulatory Affairs, and Post-Market Surveillance across lifecycle.
• Lead quality oversight of new product development, design changes, product transfers, sustaining engineering, and lifecycle initiatives.
• Drive enterprise-wide quality transformation and continuous improvement initiatives.
• Make risk-based decisions balancing patient safety, regulatory requirements, and supply continuity.
• Lead regulatory inspections, audits, and compliance activities globally.
• Develop leaders and strengthen succession planning within Quality.
• Provide executive insights and recommendations on quality performance and strategic initiatives.
• Partner with leadership to keep Quality a competitive advantage.
• Travel up to 40% to manufacturing sites and vendors.

Skills

Quality leadership

Regulatory compliance

Executive communication

Cross-functional leadership

Budget management

Education

Bachelor's degree in Engineering/Science

Advanced degree preferred

Job 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.

Your Role at Baxter

At Baxter, every quality decision has the potential to impact patients who depend on life-sustaining medical devices every day. As Senior Director, Quality - Medical Devices, you will lead Quality strategy and performance across Baxter's Infusion Therapies & Platforms (ITP) medical device network, ensuring the safety, quality, compliance, and reliable supply of products used by patients and healthcare providers around the world.

The senior Quality leader is responsible for quality strategy, governance, organizational capability, regulatory compliance, and business performance across a global medical device network. Leading a large, geographically dispersed organization, you will provide executive oversight of Design Quality, Manufacturing Quality, and Post-Market Surveillance activities across the full product lifecycle, from development through commercialization and ongoing market performance.

Success in this role means strengthening regulatory confidence, enabling reliable supply, advancing operational excellence, driving product and patient safety, and developing a high-performing organization focused on quality excellence.

What You'll Be Doing

• Develop and execute a multi-year Quality strategy that strengthens compliance, product quality, organizational capability, and business performance across Baxter's medical device network.
• Lead Quality governance and decision-making processes that promote consistency, accountability, risk management, and operational excellence across multiple sites and functions.
• Provide executive oversight for Design Quality, Manufacturing Quality, and Post-Market Surveillance activities across the medical device lifecycle.
• Partner with senior leaders across Manufacturing, R&D, Regulatory Affairs, Supply Chain, Finance, HR, and Commercial functions to support innovation, lifecycle management, and reliable product supply.
• Champion regulatory compliance and inspection readiness across global medical device operations while building strong, credible relationships with health authorities, notified bodies, and regulatory agencies.
• Ensure effective integration of Design Quality, Manufacturing Quality, Regulatory Affairs, and Post-Market Surveillance activities to support product lifecycle excellence.
• Lead quality oversight of new product development, design changes, product transfers, sustaining engineering activities, and lifecycle management initiatives.
• Drive enterprise-wide quality transformation, remediation, and continuous improvement initiatives that deliver sustainable business results.
• Make risk-based decisions that balance patient safety, product quality, regulatory requirements, supply continuity, and business objectives.
• Lead and oversee regulatory inspections, audits, and compliance activities across global medical device operations.
• Build, coach, and develop high-performing leaders while strengthening succession planning and organizational capability across the Quality organization.
• Provide executive-level insights, reporting, and recommendations related to quality performance, compliance risks, business priorities, and strategic initiatives.
• Partner with executive leadership to ensure Quality remains a competitive advantage while supporting growth, innovation, and operational excellence across the business.
• Travel up to 40% to manufacturing sites and vendors.

What You'll Bring

• 15+ years of progressive Quality leadership experience within the medical device industry, with a proven track record leading Quality strategy, compliance, governance, and organizational performance across complex manufacturing and product development environments.
• Bachelor's degree in Engineering, Science, or a related discipline required; advanced degree preferred.
• Deep expertise in medical device quality systems, regulatory requirements, inspection management, and risk mitigation.
• Demonstrated success leading Design Quality, Manufacturing Quality, and Post-Market Surveillance organizations within a regulated medical device environment.
• Strong knowledge of global medical device regulations and standards, including FDA Quality System Regulation / Quality Management System Regulation (QSR/QMSR), ISO 13485, EU MDR, MDSAP, and related requirements.
• Proven ability to influence executive stakeholders and guide high-impact business decisions.
• Demonstrated success leading quality transformation, remediation, and continuous improvement initiatives across multiple sites and functions.
• Experience leading large, geographically dispersed teams through organizational growth, change, and business transformation.
• Strong business acumen with experience managing significant budgets, investments, and strategic operating plans.
• A collaborative leadership style with a passion for developing talent, building inclusive teams, and fostering a culture of accountability and continuous improvement.

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 $216,000 - $297,000 annually. 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.

At Baxter, you'll join a team united by a shared purpose: improving outcomes for patients and healthcare providers around the world. We believe innovation happens through collaboration, diverse perspectives, and a relentless commitment to excellence. Here, your leadership will help shape the future of healthcare while creating opportunities for growth, impact, and professional fulfillment.

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.

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

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

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.