Associate Director, Quality Compliance

Reposted 14 Hours Ago
Be an Early Applicant
Round Lake, IL, USA
In-Office
152K-209K Annually
Senior level
Healthtech • Other
The Role
The Associate Director leads Quality Compliance programs, coordinating audits, inspection readiness, and regulatory updates while managing staff and compliance strategies across drug delivery operations.
Summary Generated by Built In

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

The Associate Director of Quality Compliance supports the site’s Quality Management System (QMS) and compliance programs across the Round Lake Drug Delivery network. This role provides operational leadership for audits, training, documentation, change control, and inspection readiness activities. The Associate Director partners with the Director of Quality Compliance to ensure the site maintains a robust compliance posture and proactively meets global regulatory expectations.

What you'll be doing

Compliance Program Leadership

  • Lead day‑to‑day activities within the site’s Quality Compliance programs, ensuring alignment with global regulatory requirements.

  • Support implementation of sitewide compliance strategy, policies, and standardization initiatives.

  • Monitor compliance performance and escalate issues to the Director as needed.

Inspection Readiness

  • Coordinate readiness assessments and preparation activities for regulatory inspections and corporate audits.

  • Serve as back‑room or front‑room support during inspections; manage documentation and response tracking.

  • Ensure inspection readiness across assigned buildings and shifts.

Audit Management

  • Lead internal audits, supplier audits, and follow‑up activities.

  • Support external audit planning, execution, and timely response to findings.

  • Track commitments and ensure effective CAPA implementation.

Regulatory Intelligence Implementation

  • Assist in evaluating regulatory updates and enforcement trends.

  • Translate requirements into updated procedures, training, and QMS enhancements.

Quality Systems Ownership

  • Oversee controlled documentation processes to ensure accuracy and compliance.

  • Manage training system execution, including curriculum updates, effectiveness checks, and digital training tools.

  • Lead change control processes within delegated authority and contribute to site Management Review preparation.

  • Support digital transformation and compliance‑related modernizations.

Remediation & Risk Management

  • Lead or support remediation teams focused on resolving compliance gaps and audit findings.

  • Conduct risk assessments and monitor compliance KPIs, dashboards, and analytics.

  • Identify systemic issues and partner cross‑functionally for sustainable solutions.

Cross‑Functional Collaboration

  • Work closely with QA Ops, Engineering, Manufacturing, Facilities, Supply Chain, and Regulatory Affairs.

  • Support compliance aspects of tech transfers, submissions, capital projects, and lifecycle changes.

People Leadership

  • Manage and develop Quality Compliance staff.

  • Build a culture of transparency, engagement, and continuous improvement.

What you'll bring

  • Bachelor’s degree in science or engineering required; advanced degree preferred.

  • 10+ years of experience in Quality Compliance/Quality Systems; 3–5 years leadership.

  • Recent pharmaceutical manufacturing experience is required.

  • Strong knowledge of FDA/EMA regulations, QMS elements, and audit/inspection processes.

  • Proven ability to lead audits, manage documentation systems, and drive compliance improvements

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 $152,000 - $209,000 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. 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.

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.

Top Skills

Quality Management System (Qms)
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The Company
HQ: Deerfield, IL
35,858 Employees
Year Founded: 1931

What We Do

Every day, millions of patients, caregivers and providers around the world rely on Baxter’s leading portfolio of diagnostic, critical care, nutrition, kidney care, hospital and surgical products and solutions. For 90 years, we’ve been making an impact at the critical intersection where innovations that save and sustain lives meet the healthcare providers who make it happen. With products, therapies and digital health solutions available in more than 100 countries, Baxter’s employees worldwide are now building upon the company’s rich heritage of medical breakthroughs to advance the next generation of transformative healthcare innovations. We welcome Hillrom to Baxter, where we are uniting to advance patient care worldwide. We’re building on the strengths of two historically innovative and socially responsible companies that will better serve our patients, customers and communities.

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