We are seeking a detail-oriented Validation Engineer to support validation and calibration activities for critical pharmaceutical manufacturing and sterile processing equipment.
This role requires strong expertise in regulatory compliance, including GMP and 21 CFR Part 11, along with hands-on experience in equipment qualification and computerized system validation (CSV).
Roles & Responsibilities:
Perform validation and calibration activities for pharmaceutical manufacturing and sterile processing equipment
Ensure compliance with GMP and 21 CFR Part 11 standards
Develop and execute Master Validation Plans, SOPs, and validation protocols for process validation (PPQ), aseptic processes, and cleaning/sterilization procedures
Conduct equipment qualification activities (IQ/OQ/PQ) and ongoing perform...