Quality Engineer I
Baxter · Cleveland, MS
- Level
- Engineer
- Team
- Quality
- Base pay
- $76k–$95k
- Degree
- Required
- Experience asked
- 1+ years
- Industry
- Medical devices
- Posted
- Today
The role in 30 seconds
An engineer-level quality role at Baxter (medical devices) in Cleveland, MS. Here, you will find more than just a job—you will find purpose and pride.
- They ask for
- 1+ years · degree required
- Tools it names
- Lean, FDA / GMP, Validation (IQ/OQ/PQ), PLC, Automation
- Base pay
- $76k–$95k
- Day to day
- some off-shift / weekend coverage
Read from the posting. The full description is below.
From the plant jobs report · week of November 2, 2026
Quality Engineer roles in Mississippi: typical posted base $76k–$105k. This one lists $76k–$95k.
Median of the low and high ends of 4 live postings that list pay, out of 9 quality engineer openings in Mississippi, read from manufacturers' own careers sites.
Mississippi plant jobs report →Pay by team and state →What moves pay →
How this role compares
Against 8 other live quality postings in Mississippi.
- Experience asked
- Less than usual (1+ vs 4+)
Similar roles usually ask 4+ years.
Skills these teams ask for most
- Root cause 56%
- ISO 9001 56%
- AS9100 56%
- ✓ Lean 44%
- ✓ Team leadership 44%
- ✓ Automation 33%
✓ = this posting asks for it too. % = share of similar postings that mention it.
At a glance
Pulled from the posting text. If it's not listed here, the posting didn't say.
How to get in at this plant
Five moves over a week or two. The first one takes ten minutes.
- 1
Pick 2–3 people on the Quality team at Baxter
We found 2 people at this company and state: 1 in this kind of role, 1 leaders. Engineers who joined in the last year or two reply the most. See them ↓
- 2
Send a short, curious note
One real question about their work. No favors yet. Each person gets a different note, written for this role.
Write to Michael → (free) - 3
Turn a reply into a short call
Questions worth asking about this team:
- What does a normal week look like on your team?
- Which standards drive the work here: ISO 13485, IATF 16949, AS9100?
- How much of the job is customer complaints versus prevention?
- How does off-shift and weekend coverage work?
- How did you land the job? What stood out in your interviews?
- 4
Apply with someone vouching for you
If the call went well, ask whether they’d pass your résumé to the hiring manager. Send your résumé link, apply that day, and let them know.
- 5
Bring proof to the interview
One page of before-and-after numbers from projects you led: scrap, OEE, cycle time, cost. Plant managers hire on results.
This plant: Baxter in Cleveland
4 other open roles at this site · 2 people we found in quality roles at Baxter.
- Maintenance Mechanic I - 3rd Shift · Reliability · Technician
- Senior Quality Manager · Quality · Manager
- Maintenance Mechanic I - 2nd Shift · Reliability · Technician
- Production Technician II - Molding (2nd Shift) · Production · Technician
Full description from BaxterAs posted on their careers site.ShowHide
Key Responsibilities
- ◆Perform process validation, process capability, and process control studies for assigned areas.
- ◆Drive quality/manufacturing projects by applying Lean, problem-solving, process control, and project management tools to achieve and sustain operational excellence.
- ◆Support Manufacturing, Engineering, and Quality Management departments with the development and implementation of new processes and technology.
- ◆Assist in identifying and developing process improvement projects, including automation and computerization.
- ◆Ensure computer systems and applications align with regulatory quality standards through validation activities.
- ◆Ensure FDA regulations are met for system upgrades and replacements.
- ◆Ensure the quality of facility systems by writing and completing protocols and test cases for validations. Coordinate testing and detailing of projects. Perform and deliver changes to applications and assist in training for systems.
- ◆Apply diversified knowledge of applied Statistical Analysis techniques, procedures, and criteria to carry out measurements, process, and product capability studies toward the development of new or refined equipment, materials, processes, instruments, and products.
- ◆Communicate effectively in written and verbal form and function effectively as a team member.
- ◆Align with plant and department environmental health and safety regulations.
- ◆Learn, understand, and apply rigorous quality standards, established guidelines, and current Good Manufacturing Practices (cGMP).
- ◆Notify the supervisor and take appropriate action if any safety, quality, mechanical, or discrepancy issues occur.
- ◆Sustain a clean and safe work area using 6S principles.
- ◆Perform all other duties and
responsibilities
as determined by supervision/management.
requirements
as detailed in the Baxter Cleveland Visual Acuity Procedure CL-01-01-037.
Physical
Requirements
- ✓Ability to lift up to 10 pounds.
- ✓Ability to sit, stand, and/or walk for long periods.
- ✓Ability to reach above the shoulder.
- ✓Ability to bend/stoop.
Required Education and Experience
- ✓BS degree in Engineering, Computer Science, or other core Science Field and 0-1 year related experience (in-house, co-op, or acquired outside).
Other Duties as Assigned
Please note this job description is not built to cover or contain a comprehensive listing of activities, duties, or
responsibilities
required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice. Overtime is worked as required.
Applicants must be authorized to work for any employer in the U.S. We cannot sponsor or transfer sponsorship of an employment visa.
US Benefits at Baxter (except for Puerto Rico)
Show full description ↓Show less ↑
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.
As a Quality Engineer I at Baxter Healthcare Corporation, you will have a meaningful role in ensuring the quality and reliability of our healthcare products. This is an outstanding opportunity to advance your career in a dynamic and supportive environment. Your work will directly affect the health and well-being of patients worldwide.
Knowledge, Skills, and Abilities
- •Knowledge of applications such as Wonderware, Allen-Bradley PLC, Access, and Microsoft Project preferred.
- •ASQ Certification (CQE or CSQE) or equivalent desired.
- •Strong leadership skills and the ability to work with diversified cross-functional teams across different plant locations.
- •Logical thought process and self-motivation to work well without direct supervision.
- •Ability to quickly learn and understand applications.
- •Experience in Quality Assurance or the Pharmaceutical industry desired.
- •Meet visual acuity