Quality Engineer I
Baxter · Cleveland, MS
QualityFull-time$76k–$95kCompany career page
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Role summary
Quality Engineer I role at Baxter focused on ensuring product quality and reliability through process validation, capability studies, and manufacturing projects. The position supports cross-functional teams in implementing process improvements and regulatory compliance within a healthcare manufacturing environment.
What they're looking for
- Bachelor's degree in Engineering, Computer Science, or related science field
- 0-1 year related quality assurance or pharmaceutical industry experience
- ASQ Certification (CQE or CSQE) or equivalent desired
- Knowledge of Wonderware, Allen-Bradley PLC, Access, Microsoft Project preferred
- Strong leadership and cross-functional collaboration skills
- Ability to work independently with logical problem-solving approach
What you'll be doing
- Conduct process validation, capability, and control studies for assigned manufacturing areas
- Lead quality and manufacturing projects using Lean, problem-solving, and project management tools
- Support development and implementation of new processes and technologies across departments
- Perform computer system validation activities ensuring FDA regulatory compliance
- Write protocols and test cases for facility system validations and coordinate testing activities
Privacy & handoff
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