Quality Engineer II - Medical Devices & Validation

Orchid Orthopedic Solutions LLC

Memphis (TN)

On-site

USD 85,000 - 110,000

Full time

4 days ago
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Benefits offered by this job

Performance bonuses
Insurance
401(k) with company match
Paid time off

Job summary

Orchid Orthopedic Solutions LLC in Memphis, TN seeks a Quality Engineer II to support legacy products and assist with new production introduction and validation. This role interfaces with project management and manufacturing engineers to uphold quality standards throughout development and production.

The ideal candidate brings 3+ years in manufacturing, a Bachelor’s degree, and knowledge of quality tools, PPAP processes, and validation activities, enabling strong cross-functional collaboration

Qualifications

  • Bachelor degree required.
  • 3+ years of experience in a manufacturing environment.
  • Experience in medical device manufacturing preferred.

Responsibilities

  • Completes all required training.
  • Uses quality tools to implement improvements including process flowcharting, Pareto analysis, and SPC.
  • Acts as a customer liaison and processes customer quality complaints as applicable.
  • Collects, analyzes, and presents data using statistical methods.
  • Supports measurement and analysis of key metrics to monitor performance.
  • Leads productivity improvements and continuous improvement projects.
  • Reviews and approves product/process and document change requests.
  • Participates in pre- and post-production launch reviews.

Skills

Statistical Analysis
Quality Management
Process Management
Lean Manufacturing
PPAP
Problem Solving

Education

Bachelor's degree
B.S. in a related field

Job description

Orchid Orthopedic Solutions LLC in Memphis, TN seeks a Quality Engineer II to support legacy products and assist with new production introduction and validation. This role interfaces with project management and manufacturing engineers to uphold quality standards throughout development and production.

The ideal candidate brings 3+ years in manufacturing, a Bachelor’s degree, and knowledge of quality tools, PPAP processes, and validation activities, enabling strong cross-functional collaboration

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