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Mgr II, Quality Assurance - Solutions

Job in Cleveland, Bolivar County, Mississippi, 38733, USA
Listing for: Baxter International
Full Time position
Listed on 2026-03-12
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering
  • Engineering
    Quality Engineering
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 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.

About the Company

Join Baxter Healthcare Corporation, where our innovative technology and automation lead the healthcare industry. Located in Cleveland, MS, our facility is the U.S. sole source for several critical medical products and has been vital to Baxter for over 60 years. We take pride in our diverse automated manufacturing technologies, such as bottle solution filling, injection molding, and device assembly. Here, you will find a challenging and rewarding work environment that offers competitive compensation and benefits.

We encourage a culture of inclusion and collaboration. Together, we can advance healthcare for patients worldwide, crafting work you can be proud of!

About the Position

As the Manager II, Quality Assurance - Solutions, you will lead all aspects of Devices Quality operations and manage staff in this area. You will direct, coordinate, and evaluate the unit's work, ensuring activities follow company policies and legal requirements. You will also lead initiatives to improve processes and maintain compliance with standards, ensuring our products meet quality expectations.

Essential Duties and Responsibilities
  • Lead quality oversight for the Devices areas.
  • Develop, assign, and implement systems, procedures, and policies to ensure compliance with ISO Standards, cGMP's, FDA regulations, and company policies.
  • Conduct audits and implement changes to specifications, SOPs, and forms for regulatory compliance and process improvement.
  • Ensure product compliance through established inspection criteria and procedures.
  • Coordinate inspection activities throughout the production cycle.
  • Analyze statistical data and product specifications to determine and improve quality standards.
  • Prepare and submit reports to Managers and other Departments or Agencies as required.
  • Communicate quality philosophy to key personnel.
  • Actively participate in quality management teams within the organization.
  • Manage and support area associates, encouraging a teamwork environment.
  • Train and integrate new engineers, associates, and technicians.
  • Drive quality/manufacturing projects using Lean, problem‑solving, process control, and project management tools.
  • Maintain comprehensive knowledge of plant systems, processes, procedures, documentation, and products.
  • Evaluate and implement system changes per Baxter procedures.
  • Lead and establish effective working teams.
  • Manage and prioritize multiple tasks and projects.
  • Ensure effective communication in both written and verbal forms.
  • Coordinate financial goals and budgets for departments.
  • Promote company security, industrial hygiene, cGMPs, and other established policies.
  • Perform tasks independently with minimal supervision.
  • Travel as needed to fulfill duties.
Qualifications
  • Bachelor’s degree in Microbiology, Biology, Chemistry, or Engineering, or equivalent experience, required.
  • 5+ years of Engineering/Manufacturing/Quality experience required, with 3‑5 years of leadership experience.
  • FDA regulated manufacturing experience preferred.
  • Six Sigma Green Belt Certification or industry‑standard equivalent preferred.
  • Project Management skills and experience are preferred.
  • Experience and skills in Lean Manufacturing are preferred.

We understand that 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.…

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