Executive

Education: B. Pharma

Experience: Min 8 years in Pharma (MDI / DPI / Derma & Nasal) (USFDA exposure mandatory)

CTC: 10–12 LPA

Key Responsibilities:

• Preparation and review of Validation Master Plan, Cleaning Validation Master Plan, Protocols & Reports

• Execution of Cleaning Validation Protocols, Cleaning Validation Matrix, Cleaned & Dirty Equipment Hold Time Studies

• Performing Equipment Qualification (manufacturing & packing)

• Conducting Temperature & RH Mapping of storage areas

• Performing Utility Qualification – Compressed Air, Nitrogen Gas, Purified Water System

• Facility & HVAC Qualification, including periodic HVAC validation

• Handling regulatory, customer, and internal audits, and ensuring timely compliance