CareerPlan

Change Control and Quality Systems Specialist

Greenville, North Carolina, USAFull-time2026-10-14 → 2026-11-10
No visa sponsorship

Core

Ensuring quality and compliance within regulated environments while supporting continuous improvement and operational excellence across quality systems.

Role type

Quality Systems Specialist (Pharmaceutical/Medical Device)

Builds

Quality documentation, compliance reports, and continuous improvement initiatives

Domain

Pharmaceutical/Medical Device Manufacturing

Required skills

GMP/GxP compliance, Change Control management, CAPA management, Deviation management, Audit support, SOP development, Data analysis, Risk assessment, Continuous improvement tools, Quality systems software proficiency

Preferred skills

Pharmaceutical industry experience, Change management experience, Project management, Medical device change management, Power BI/Tableau proficiency