Casting Quality Control Inspector

Boulder Connect

Tualatin (OR)

On-site

USD 25,000 - 39,000

Full time

26 hours ago
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Job summary

Boulder Connect is seeking a Visual Inspector, Rough Casting to support the manufacturing of orthopedic products. This on-site role requires meticulous inspection of rough castings to ensure conformity with specifications and quality criteria.

You will use inspection tools, document results, and report nonconforming materials for review. Collaborative work with production and quality teams will promote a safe, organized environment and continuous improvement within a regulated medical-device

Qualifications

  • Attention to detail is essential for defect detection and reporting.
  • Strong documentation skills are required to accurately record inspection results.
  • A demonstrated commitment to quality within a regulated medical-device manufacturing setting is expected.

Responsibilities

  • Visually inspect rough castings for defects.
  • Verify that parts meet established specifications and quality criteria.
  • Use inspection tools and work instructions to perform checks.
  • Accurately document inspection results.
  • Report nonconforming materials for review.
  • Collaborate with production and quality teams to maintain a safe, organized work environment and support continuous improvement.

Skills

Attention to detail
Documentation skills
Commitment to quality

Tools

Inspection tools

Job description

We are seeking a Visual Inspector, Rough Casting to support the manufacturing of orthopedic products.
In this on-site role, you will

  • visually inspect rough castings for defects
  • verify that parts meet established specifications and quality criteria
  • use inspection tools and work instructions
  • accurately document inspection results
  • report nonconforming materials for review
Collaborate with production and quality teams to maintain a safe and organized work environment and support continuous improvement.
Candidates should demonstrate attention to detail, dependable documentation skills, and a commitment to quality within a regulated medical-device manufacturing setting.
Training and cross-functional collaboration opportunities are available to enhance your technical expertise.
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