Sr. Analyst, Quality Systems

Baxter International Inc. • Saint Paul, MN

3d • Onsite

About The Position

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.

Requirements

• Demonstrates strong verbal and written communication skills, applying effective documentation practices and engaging confidently across all levels of the organization.
• Drives continuous improvement of procedures and processes, simplifying complexity, increasing efficiency, and enhancing usability across Quality Systems.
• Interprets and applies quality system regulations, ensuring compliance and translating regulatory requirements into practical, site-ready solutions.
• Maintains relevant professional certifications (e.g., CQA, ISO 13485 Auditor), or actively works toward certification to strengthen technical expertise.
• Fosters a collaborative, team-oriented environment, building strong relationships and influencing others through effective interpersonal and leadership skills.
• Applies strong problem-solving and critical-thinking skills, with a high level of attention to detail and the ability to clearly communicate findings and recommendations.
• Manages projects effectively, prioritizing work, meeting deadlines, and ensuring successful execution of multiple concurrent initiatives.
• Demonstrates working knowledge of FDA and ISO regulations, including ISO 13485 and 21 CFR 820, and ensures consistent application of Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP).
• Bachelor’s degree in science or engineering or other related field
• Minimum of 5+ years of experience in Quality with emphasis on regulation and compliance, or related field in the medical device industry.
• Audit experience (as auditee or auditor) required

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 strategic initiatives as needed, supporting site and organizational priorities.
• Supervise team members
• Other duties, tasks or projects as assigned.

Benefits

• medical and dental coverage that start on day one
• insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
• Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount
• 401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching
• Flexible Spending Accounts
• educational assistance programs
• paid holidays
• paid time off ranging from 20 to 35 days based on length of service
• family and medical leaves of absence
• paid parental leave
• commuting benefits
• Employee Discount Program
• Employee Assistance Program (EAP)
• childcare benefits

What This Job Offers

• Job Type: Full-time
• Career Level: Senior