Staff Engineer - Quality Document Systems

BD

Durham, North Carolina, United States
On-site (minimum of 4 days in office per week)
Quality management system (qms) oversight
Document and change management
Compliance to regulations and standards
BD is seeking a Staff Engineer - Quality Document Systems in Durham, North Carolina, to oversee and improve document and change management processes within their Quality Management System (QMS). The ideal candidate should have extensive experience in QMS administration, particularly in the medical device or life sciences sectors

Job Summary

  • The Staff Quality Document Systems Management Engineer is responsible for technical oversight and continuous improvement of document and change management processes within the Quality Management System (QMS).
  • The role supports broader QMS activities including compliance, audit readiness, and process optimization, monitoring QMS activities, managing audits, and implementing quality control measures.
  • BD is one of the largest global medical technology companies in the world, advancing the world of health through transformative solutions.

Matching Summary

Match Score: 85

BD is seeking a Staff Engineer - Quality Document Systems in Durham, North Carolina, to oversee and improve document and change management processes within their Quality Management System (QMS). The ideal candidate should have extensive experience in QMS administration, particularly in the medical device or life sciences sectors.

Skills & Requirements

Must-have

  • Quality Management System (QMS) oversight
  • document and change management
  • compliance to regulations and standards
  • Learning Management System (LMS) administration
  • electronic documentation systems SME

Nice-to-have

  • collaboration with diverse teams
  • actionable insights from observations
  • strategic corrective action plans
  • consistency across quality practices

Key Requirements

  • Bachelor's degree in a relevant field
  • 10 years' experience in QMS administration, change management, document control, audit management
  • 8 years of medical device or life science industry experience
  • Demonstrated experience in managing audits and CAPAs

Work Rights

Not specified

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