2nd Shift QC Inspector, Medical Devices

MicroPort Orthopedic

Arlington (TN)

On-site

USD 42,000 - 64,000

Full time

14 days+
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Benefits offered by this job

Medical
Dental
Vision
401(k) match
PTO
Paid Holidays
Employee Assistance Program

Job summary

MicroPort Orthopedic in Arlington, TN is seeking an Associate Quality Control Inspector for the 2nd shift (3:00-11:30pm, Monday-Friday). You will inspect materials, components and finished devices to ensure specifications are met and adhere to FDA/ISO guidelines.

Strong attention to detail and teamwork are essential for accurate documentation and inspection outcomes. You will interact with engineers and auditors, follow engineering instructions, and contribute to a compliant quality environment.

Qualifications

  • Inspect raw materials, components and finished products to ensure conformance to specification.
  • Follow written instructions with engineering-based content.
  • Train in mechanical inspection techniques.

Responsibilities

  • Ensure inspection is performed in accordance with FDA, ISO, and other applicable regulations/guidelines.
  • Follow written instructions with engineering-based content.
  • Train in mechanical inspection techniques.
  • Apply attention to detail for medical device product features.
  • Interface with peers, engineers, and Regulatory auditors.
  • Record inspection results accurately to ensure proper segregation of accepted and rejected products.

Skills

Quality inspection
Attention to detail
FDA/ISO compliance
Teamwork
Documentation

Education

High School Diploma or GED

Job description

MicroPort Orthopedic in Arlington, TN is seeking an Associate Quality Control Inspector for the 2nd shift (3:00-11:30pm, Monday-Friday). You will inspect materials, components and finished devices to ensure specifications are met and adhere to FDA/ISO guidelines.

Strong attention to detail and teamwork are essential for accurate documentation and inspection outcomes. You will interact with engineers and auditors, follow engineering instructions, and contribute to a compliant quality environment.

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