Top 2 Supplier quality engineer Jobs in Fort Smith Ar

Principal Quality Engineer
Katalyst Healthcares & Life Sciences —Fort Smith, AR
- Contract
- Hybrid work
- Engineering
- 8 years
- Mentoring
Quick Apply
Supplier Quality - Packaging
Wells Enterprises —United States
- $93,959.91 - $131,543.88 a year
- Full-time
- 6 years
- Research
- Bachelor's degree

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Walther Manufacturing is looking for a Senior Design Engineer with experience in the field of firearm design and development.
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Supplier Quality Engineer
Nifco America, Corp. —Canal Winchester, OH
ASQ or equivalent certification or training (CQE, LSS Belt, etc). IATF certification for Internal or Lead auditor with documentation available.
$70,000 - $88,000 a year
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9d
Supplier Quality Engineer
Honda —Raymond, OH
Provide technical assessment and support throughout tool trials and crisis activity, as needed. Prepare, develop, and manage approval of part conformance prior…
$71,100 - $106,600 a year
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Principal Quality Engineer

Katalyst Healthcares & Life Sciences -
Fort Smith, AR

Quick Apply

Job Details

Contract

Qualifications

Statistics
Engineering development testing
Managing projects in an engineering role
Quality control statistical data analysis
Statistical Process Control
Six Sigma methodology implementation
Engineering process optimization
Corrective and preventive actions (CAPA)
GMP
ISO certification audits
Change management
Bachelor's degree in engineering
Production validation processes
Quality risk management
Design failure mode and effects analysis (DFMEA)
Mentoring
Leading team collaboration initiatives
Regulatory/legal compliance standards in production
Design controls
Biomedical regulatory compliance
Operational excellence initiatives
Manufacturing
Quality improvement programs in engineering
Cross-functional team management
Implementing lean manufacturing processes
Cross-functional communication
FDA regulations
Failure analysis

Full Job Description

Job Description:
We are seeking an experienced Principal Quality Engineer to lead quality engineering initiatives that ensure compliance, product quality, and continuous improvement across manufacturing and product development processes. The ideal candidate will provide technical leadership in quality systems, risk management, validation, CAPA, supplier quality, and regulatory compliance while partnering with cross-functional teams to drive operational excellence.
Responsibilities:

Lead quality engineering activities supporting product development, manufacturing, and sustaining engineering.
Develop and implement quality strategies that comply with FDA, ISO 13485, ISO 9001, and other applicable regulatory requirements.
Drive root cause investigations and corrective and preventive actions (CAPA) using structured problem-solving methodologies.
Lead risk management activities including DFMEA, PFMEA, risk assessments, and mitigation plans.
Review and approve engineering change orders (ECOs), design documentation, validation protocols, and quality records.
Support design control activities including Design Verification & Validation (V&V), Design Reviews, and Design History Files (DHF).
Analyze quality metrics and implement continuous improvement initiatives using Lean Six Sigma and statistical tools.
Lead process validation activities including IQ, OQ, PQ, and process capability studies.
Collaborate with Manufacturing, R&D, Regulatory Affairs, Supply Chain, and Operations to resolve quality issues.
Provide technical leadership during internal, customer, and regulatory audits.
Mentor and coach Quality Engineers and cross-functional teams on quality best practices.
Support supplier qualification, supplier audits, and supplier quality improvement initiatives.
Ensure compliance with cGMP, FDA Quality System Regulation (21 CFR Part 820/QMSR), and applicable international standards.

Requirements:

Bachelor's degree in Engineering (Mechanical, Biomedical, Industrial, Manufacturing, Electrical, Chemical, or related discipline).
8+ years of Quality Engineering experience in a regulated manufacturing environment.
Strong knowledge of FDA regulations, ISO 13485, ISO 9001, and cGMP requirements.
Experience with Design Controls, Risk Management (ISO 14971), CAPA, Client, and change management.
Hands-on experience with process validation (IQ/OQ/PQ), statistical analysis, SPC, MSA, and capability studies.
Strong knowledge of Lean Manufacturing, Six Sigma, and continuous improvement methodologies.
Excellent root cause analysis skills utilizing 8D, Fishbone, 5 Whys, and similar tools.
Experience leading cross-functional projects and mentoring engineering teams.
Strong written, verbal, and presentation skills.

Preferred Qualifications:

Master's degree in Engineering or related technical field.
ASQ Certified Quality Engineer (CQE), Six Sigma Green Belt or Black Belt.
Experience in medical devices, pharmaceuticals, biotechnology, aerospace, automotive, or other highly regulated industries.
Experience supporting FDA inspections and ISO certification audits.
Knowledge of validation documentation, statistical software (Minitab), and quality management systems.

Quick Apply

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supplier quality engineer jobs in fort smith ar

Principal Quality Engineer

Supplier Quality - Packaging

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