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QA Manager

Clayton,United States💼 Full-time🗓 2026-08-07 → 2026-09-26

Core

Lead Regulatory, Quality Control, and Quality Assurance activities to ensure product release decisions and customer quality requirements are met in a manufacturing environment.

Role type

Senior IC QA Manager (manufacturing)

Builds

Quality Management Systems, audit readiness, and compliant product releases

Domain

Manufacturing (Printing and Packaging) with Pharmaceutical/Healthcare customers

Deliverable

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

Required skills

GMP compliance, Quality Management Systems management, CAPA management, root cause analysis, supplier qualification, audit leadership, team management, data integrity, risk assessment, change control

Preferred skills

ISO 9001:2015 Lead Auditor certification, BRCGS Packaging Lead Auditor certification, Six Sigma Green Belt, experience in Printing and Packaging industry, experience supporting Pharmaceutical/Healthcare customers, data analytics for quality metrics

Technologies

eQMS, calibration systems

Responsibilities

Lead customer audit readiness activities including preparation, hosting, and closing findings; manage customer complaints, investigations, and root cause analysis; oversee batch quality control testing and product release activities; approve raw materials, components, in-process materials, finished products, and labeling; manage supplier qualification, audits, and performance; maintain and improve Quality Management Systems; develop GMP and Quality Systems training programs; lead, coach, and develop the Site Quality team

Seniority

Senior, hands-on IC

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