Putta Sreenivas
Qa Compliance Specialist @AbbVie
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WORK HISTORY
Qa Compliance Specialist @AbbVie
IE
ABOUT PUTTA SREENIVAS
Pharmaceutical professional with over 8 years of combined experience in Quality Assurance Compliance, Aseptic Manufacturing Quality Oversight, and Validation (CQV / CSV) within sterile manufacturing environments.Currently supporting aseptic manufacturing operations at AbbVie, Westport (Ireland), providing quality oversight, real-time documentation review, and aseptic behavior monitoring under EU GMP and HPRA guidelines.Previously delivered extensive Commissioning, Qualification, and Validation (equipment, utilities, and computerized systems) for sterile facilities with Viatris, Alembic Pharmaceuticals, and Aurobindo Pharma.Skilled in GMP compliance, deviation and CAPA management, QMS, risk assessment, and audit readiness, with a strong focus on continuous improvement and maintaining a culture of aseptic excellence.
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