Quality professional with 16 years of progressive experience with sound knowledge in Quality systems of Generic pharmaceutical industry. Extensive experience ensuring quality in related manufacturing pharmaceutical products. Expertise in non-compliance investigations, Deviations, CAPA, Change control management systems, Facility audits and Quality management systems. Working knowledge in Track Wise, SAP and MS office. Excellent organization and communication skills with a reputation for multi-tasking and solving problems in fast-paced environments. Quality management systems * CAPA * Good manufacturing practices (cGMP) * Review of Batch records and Protocols * Change control management system * Audit and compliance * Deviations * Validations

Highlights:

• Packaging
• Quality Assurance
• Risk Assessment
• Test
• Change Control
• Documentation
• Management
• Product Development
• Risk Management
• Development Activities