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Pharmaceutical Professional, GMP Compliance,CAPA,Risk assesment, validatoin,SOPs
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Quality Assurance executive
Abbott • Temps plein
Jun 2026 - Present • 0 mos
Managed GMP documentation and quality system records. Prepared, reviewed and controlled SOPs. Monitored deviation investigation, root cause analysis and CAPA implementation. Conducted risk assessment and supported quality improvement initiatives. Reviewed batch manufacturing and packaging records for compliance. Assisted in internal and external audits. Maintained documentation in accordance with GMP and data integrity requirements. Supported validation and qualifications activities.