GlaxoSmithKline in Marietta seeks a Senior QA Documentation Systems Specialist to oversee cGMP quality systems, drive data integrity, and ensure regulatory readiness for vaccine manufacturing. You will lead system ownership, KPI development, and risk-based assessments while collaborating with cross-functional teams to strengthen quality governance.
You will mentor staff, coordinate training, and support inspection responses while maintaining strong data controls and process improvements.
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Senior QA Documentation Systems Lead - Hybrid
GlaxoSmithKline · Marietta, PA, USA ·
- Job type:
- Full Time