Quality Engineer I – Medical Device QA & Process

Arthrex GmbH; Pendleton (SC); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Medical, Dental and Vision Insurance

Company-Provided Life Insurance

Voluntary Life Insurance

Flexible Spending Account (FSA)

Matching 401(k) Retirement Plan

Annual Bonus

Wellness Incentive Program

Free Onsite Medical Clinics

Free Onsite Lunch

Tuition Reimbursement Program

Paid Time Off

Employee Assistance Program (EAP)

Job summary

Arthrex, Inc. is seeking a Quality Engineer I for our Pendleton, SC manufacturing site. A bachelor’s degree in Engineering or Engineering Technology is required. The role supports QA with root-cause analysis, DHR reviews, and development of quality inspection standards.

Responsibilities include executing quality programs, data analysis, reporting, and training. Prior medical device experience is preferred; PC tools like Excel/Word are used daily.

Qualifications

• Bachelor’s degree in engineering required.
• Experience in a medical device company preferred.
• Knowledge of testing equipment and control plans.
• Strong data analysis and documentation skills.

Responsibilities

• Assist the QA department to prevent quality discrepancies and drive corrective action with guidance from Quality Engineers.
• Review DHR, inspection, functional testing, and write evaluation reports.
• Develop standards and methods for inspection, testing and evaluation.
• Design sampling procedures and forms for recording, evaluating and reporting quality data.
• Participate in training materials and sessions on quality control activities.

Skills

Quality Assurance

Root Cause Analysis

Statistical Methods

Documentation

Quality Control

Education

Bachelor's degree in Engineering

Tools

Excel

Word

QAD

Job description

Arthrex, Inc. is seeking a Quality Engineer I for our Pendleton, SC manufacturing site. A bachelor’s degree in Engineering or Engineering Technology is required. The role supports QA with root-cause analysis, DHR reviews, and development of quality inspection standards.

Responsibilities include executing quality programs, data analysis, reporting, and training. Prior medical device experience is preferred; PC tools like Excel/Word are used daily.