New · posted Oct 14
Baxter · Medical Devices
Manager, Regulatory Affairs
- Deerfield, IL
- Hybrid
- Full-time
- Manager
Open until filled
The role
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.
What you need
Minimum Requirements
- Bachelor's degree in a scientific discipline or equivalent.
- 5+ years of Regulatory Affairs experience or related experience within a regulated industry.
- Experience leading projects, cross-functional initiatives, and/or people management responsibilities.
- Knowledge of global regulatory requirements, guidance documents, and compliance expectations.
- Strong understanding of product lifecycle management and regulatory submission processes.
- Demonstrated ability to assess regulatory risks and develop effective mitigation strategies.
- Strong communication, presentation, and stakeholder management skills.
- Ability to manage multiple priorities and deliver results in a fast-paced environment.
- Experience collaborating effectively within cross-functional and global teams.
- Experience working directly with global health authorities and regulatory agencies.
- Experience supporting complex product development programs and marketed product portfolios.
- Demonstrated success leading regulatory strategy for global submissions and approvals.
- Experience representing Regulatory Affairs in industry organizations, trade associations, or external working groups.
- Prior people management experience with responsibility for coaching and developing team members.
- Experience working in multinational and multicultural business environments.
$5,000 sign‑on bonus offered for this role.
The $5,000 sign‑on bonus will be paid to external applicants successfully hired after completion of your first 30 days at Baxter.
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 $120,000 - $165,000 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. 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.
Baxter is committed to supporting the needs for flexibility in the workplace. We do so through our flexible workplace policy which includes a required minimum number of days a week onsite. This policy provides the benefits of connecting and collaborating in-person in support of our Mission. The flexible workplace policy is subject to local laws and legal requirements. At its discretion, Baxter may decide to adjust, suspend, or discontinue as business needs change.
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.
What you'll do
Your role at Baxter
As a Manager, Regulatory Affairs, you will develop and execute regulatory strategies that support business objectives throughout the product lifecycle. You will lead regulatory activities for a portfolio of products, ensuring compliance with global regulatory requirements while providing strategic guidance for product development, lifecycle management, and cross-functional initiatives. This role serves as a key liaison between Baxter, regulatory authorities, and internal stakeholders to drive successful regulatory outcomes.
- Develop and execute regulatory strategies aligned with business objectives for new product development and lifecycle management activities.
- Lead regulatory activities for assigned product portfolios, ensuring timely submissions, approvals, and compliance commitments.
- Identify regulatory risks, assess potential impacts, and implement mitigation strategies to support project success.
- Monitor global regulatory requirements and ensure compliance with applicable regulations, standards, and Baxter procedures.
- Conduct regulatory gap assessments and implement process improvements to enhance compliance and operational efficiency.
- Develop, document, and defend regulatory positions and recommendations based on sound regulatory and scientific principles.
- Serve as the primary regulatory contact with health authorities and support regulatory communications and interactions.
- Partner with cross-functional teams to align regulatory strategies, timelines, and deliverables with business objectives.
- Provide strategic regulatory guidance throughout product development and lifecycle management activities.
- Review and contribute to regulatory-related procedures and documentation to ensure alignment with evolving global requirements.
- Represent Baxter in industry associations, trade organizations, and external working groups as appropriate.
- Lead, coach, and develop regulatory team members while fostering a collaborative and high-performing environment.
Pay
$120,000 – $165,000 a year
Employer providedThis 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
Where you'll work
Deerfield, ILHybridOpen in Maps (opens in a new tab)
More jobs in Deerfield, ILEqual opportunity, accessibility and legal noticesBaxter's statements, word for word
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 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.
Job intelligence
The context around this role
Live data · October 14, 2026
Salary intelligence
How the pay compares
This role's midpoint is 14% below the US median for Regulatory Affairs roles at this level.
This roleEmployer provided
Manager roles in the US38 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $120,000 | — | $165,000 |
| All US (middle half) | $149,500 | $164,750 | $178,750 |
This role: Baxter's own published range. Comparisons: the base pay employers published on open Regulatory Affairs roles at the same level on Regulatory Jobs, October 14, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Regulatory Affairs
The general path across 201 open Regulatory Affairs roles on Regulatory Jobs, with the titles they carry most. Not Baxter's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 37 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Collaboration and leadership11
- GMP and compliance5
- Regulatory submissions5
- Documentation and SOPs4
- Quality systems and risk1
Company hiring pulse
Baxter on Regulatory Jobs
- 29
- Open roles
- 28
- Distinct roles
- 9
- Locations
By discipline
- Quality25 86%
- Regulatory3 10%
- Compliance & Safety1 3%
By level
- Associate & Specialist13 45%
- Manager6 21%
- Senior & Principal5 17%
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Manager, Regulatory Affairs at Baxter
Open until filled. $120K–$165K a year, employer provided.