Engineer Iii, Supplier Quality

Enable Injections

Cincinnati, , United States
On-site
Supplier corrective action request navigation
Corrective action preventative action navigation
Nonconformance deviation investigations
Enable Injections is seeking an Engineer III for Supplier Quality, ideally with a background in science, health, or engineering, and experience in FDA-regulated environments. The role requires a minimum of four years of relevant experience, focusing on supplier interactions in the medical device or pharmaceutical sectors, and includes responsibilities related to supplier qualification, quality audits, and documentation

Job Summary

  • Maintain the Approved Supplier List (ASL) and support ASL activities.
  • Navigate SCARs and / or Quality Alerts with the Enable team and suppliers to ensure robust documentation and closure.
  • Develop and nurture strong collaborative relationships with the Enable supplier network to support continuous improvement efforts.

Matching Summary

Match Score: 85

Enable Injections is seeking an Engineer III for Supplier Quality, ideally with a background in science, health, or engineering, and experience in FDA-regulated environments. The role requires a minimum of four years of relevant experience, focusing on supplier interactions in the medical device or pharmaceutical sectors, and includes responsibilities related to supplier qualification, quality audits, and documentation.

Skills & Requirements

Must-have

  • Supplier Corrective Action Request navigation
  • Corrective Action Preventative Action navigation
  • Nonconformance Deviation investigations
  • Quality Audit response preparation
  • Change Control Change Management navigation
  • Technical Writing ability
  • Adaptable Communication ability

Nice-to-have

  • Business Acumen strategic planning
  • Positive influence supplier leadership
  • Operate with highest integrity
  • Nurture collaborative relationships

Key Requirements

  • Bachelor’s Degree in Science, Health, or Engineering
  • Minimum four years supplier interacting experience
  • Minimum four years FDA regulated environment experience
  • Experience with medical device or pharmaceutical quality standards

Work Rights

Not specified

Tailored Resume

Cover Letter