Validation Engineer
United Pharma
Responsibilities Manage qualification and lifecycle activities for QC laboratory instruments and software systems Author and execute URS, DQ, IQ/OQ protocols, validation plans, risk assessments, and summary reports Perform Computer System Validation (CSV) activities and software testing Support change controls, deviations, investigations, and CAPA implementation Maintain asset management records, calibration schedules, and preventive maintenance activities Coordinate with vendors for installation, qualification, and troubleshooting activities Qualifications Bachelor's or Master\'s degree in Engineering, Biology, Chemistry, or related field 2–4+ years of Validation, CSV, or laboratory systems experience in a GMP environment Strong knowledge of cGMP, 21 CFR Part 11, GAMP, Data Integrity, and Electronic Records requirements Experience with change controls, deviations, investigations, and quality systems Familiarity with laboratory instruments, computerized systems, and validation documentation #J-18808-Ljbffr United Pharma
Vacancy posted 2 days ago
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