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QA Supervisor (1 Day Shift & 2 Night Shift Positions)

Greenville, North Carolina, USA💼 Full-time🗓 2026-06-26 → 2026-07-31

Core

Lead and develop a team of quality professionals while overseeing quality operations including batch record review, quality monitoring, and continuous improvement initiatives in a pharmaceutical manufacturing environment.

Role type

QA Supervisor

Builds

Ensures product quality and regulatory compliance for sterile injectable and oral solid dose drug products

Domain

Pharmaceutical manufacturing / Quality Assurance

Deliverable

production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work

Required skills

cGMP regulations, ISO standards, quality risk management, batch record review, deviation management, CAPA systems, regulatory inspections, quality training delivery, quality management software (TrackWise, SAP), validation principles

Preferred skills

Advanced degree, CQE or ASQ certification, Biology/Chemistry/Engineering background

Technologies

TrackWise, SAP

Responsibilities

Lead and develop a team of quality professionals, oversee batch record review and quality monitoring, host regulatory inspections and customer audits, implement quality improvements and leading change initiatives

Seniority

Mid-level Supervisor

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