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Sr. Analyst, Quality Systems

Job in Saint Paul, Ramsey County, Minnesota, 55199, USA
Listing for: Baxter International Inc.
Full Time position
Listed on 2026-07-14
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist, QA Specialist - Analyst/Manager
Salary/Wage Range or Industry Benchmark: 110000 - 140000 USD Yearly USD 110000.00 140000.00 YEAR
Job Description & How to Apply Below

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.

Summary

This role owns and advances key Quality Systems, including Training, Document Control, Change Control, Management Review, and Quality Audits, ensuring they are consistently implemented, compliant, and effective. The position applies a strong understanding of medical device regulations to drive compliance, improve system performance, and sustain inspection readiness across all assigned areas. This individual manages multiple priorities and projects simultaneously, operating with a high degree of accountability while effectively partnering with stakeholders at all levels of the organization.

The role requires active collaboration and influence across the enterprise, including engagement with Corporate partners, other Baxter sites, and internal and external auditors. The position also works cross-functionally with site teams—including Product Development, Process Development, QC, Manufacturing, and Quality Operations—to ensure alignment, resolve issues, and drive continuous improvement.

Essential Duties and Responsibilities
  • Own and continuously improve the site Quality Management System (QMS), ensuring alignment with regulatory requirements, ISO 13485 standards, and evolving business needs.
  • Lead the implementation, administration, and ongoing effectiveness of Quality Systems, ensuring procedures, standards, and tools are consistently applied and optimized.
  • Drive document control excellence by authoring, reviewing, and approving controlled documents to ensure accuracy, compliance, consistency, and timely periodic review.
  • Manage and enhance the training program, ensuring system effectiveness, compliance with requirements, and continuous improvement of training processes and user experience.
  • Ensure site-wide compliance readiness by coordinating internal and external audits, maintaining certifications, supporting regulatory requirements, and managing field actions.
  • Lead Management Review processes, including compiling performance data, developing presentations, facilitating discussions, and driving closure of resulting action items.
  • Own the Change Control process, conducting assessments, ensuring appropriate approvals, and driving timely execution and closure of changes.
  • Develop, monitor, and communicate Quality System metrics, identifying trends, highlighting risks, and driving data‑driven improvements.
  • Interpret and communicate QMS KPIs, ensuring leadership has clear visibility into system performance and areas requiring action.
  • Author, review, and continuously improve SOPs and controlled documents, ensuring alignment with corporate, divisional, site, and regulatory expectations.
  • Lead and deliver Quality Systems training, serving as a subject matter expert to coach and mentor individuals and teams on regulatory expectations and best practices.
  • Initiate and own nonconformance records (NCRs) as needed, supporting investigations to ensure robust root cause analysis and effective resolution.
  • Plan and execute internal audits, and coordinate, host, and respond to external audits, ensuring the site maintains a constant state of inspection readiness.
  • Drive cross‑functional collaboration to resolve compliance gaps, supporting global and site initiatives and embedding sustainable improvements.
  • Lead or contribute to multi‑site Quality projects, ensuring alignment, execution, and successful delivery of shared objectives.
  • Execute additional responsibilities and…
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