Job-ID32192212Reference26-00489 Job Summary: 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 performance monitoring Perform instrument calibration for equipment such as dual display light meters, open air shakers, and various scales Support validation of sterilization and cleaning systems, including CIP Skids, isolators, parts washers, and autoclaves Execute validation projects, ensuring timelines, budgets, and KPIs are met Collaborate with manufacturing, quality, and engineering teams to troubleshoot issues and resolve validation discrepancies Apply a risk-based approach to validation to ensure compliance and operational efficiency Coordinate resources and activities for complex validation and CSV initiatives Experience: Experience in validation, calibration, or CQV within a pharmaceutical or regulated environment Strong knowledge of GMP and 21 CFR Part 11 compliance Proven experience with Computerized System Validation (CSV) Hands-on experience with IQ/OQ/PQ and validation lifecycle documentation Strong problem-solving, communication, and cross-functional collaboration skills
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