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OBJECTIVE:    To enhance life of People by improving their health through various professional roles in Regulated Manufacturing environment, following cGMP Standards and Guidelines from FDA,EU,ICH, utilizing amazing Technologies and work together with Subject Matter Experts.

ACHIEVEMENTS:

Commissioned, Validated and Qualified 13 Manufacturing lines
Running Manufacturing Operations – PRODUCTION, ENGG & MANAGEMENT Role
Quality Audits and Compliance – FDA,EU,ICH, NOVARTIS GLOBAL, BSi, ISO audits

AREA OF ACCOMPLISHMENT
Manufacturing Operations
Validation and Qualification
Engineering, Science & Technology
Quality Assurance & Control
Quality Systems – Regulatory & Compliance

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