Quality Engineer I

Cleveland, Mississippi💼 Full-time💰 $76,000–$76,000🗓 2026-08-12 → 2026-09-29

Core

Ensure quality and reliability of healthcare products through process validation, control studies, and regulatory compliance.

Role type

Entry-level Quality Engineer (Manufacturing/Pharma)

Builds

Healthcare products and manufacturing processes

Domain

Healthcare / Pharmaceutical Manufacturing

Required skills

Process validation, process capability studies, process control, Lean problem-solving, project management, statistical analysis, cGMP knowledge, FDA regulations compliance, system validation protocols

Preferred skills

Wonderware, Allen-Bradley PLC, Microsoft Access, Microsoft Project, ASQ Certification (CQE/CSQE), Pharmaceutical industry experience

Technologies

Wonderware, Allen-Bradley PLC, Microsoft Access, Microsoft Project

Responsibilities

Perform process validation and control studies; drive quality/manufacturing projects using Lean tools; support development of new processes and technology; ensure computer systems align with regulatory standards; apply statistical analysis for product capability studies; maintain clean and safe work areas using 6S principles.

Seniority

Junior, 0-1 year experience

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About Baxter

Baxter is committed to supporting the needs for flexibility in the workplace. We do so through our flexible workplace policy which includes a required minimum number of days a week onsite. This policy provides the benefits of connecting and collaborating in-person in support of our Mission. The flexible workplace policy is subject to local laws and legal requirements. At its discretion, Baxter may decide to adjust, suspend, or discontinue as business needs change.