Validation Technician IV

Role: Validation Technician supporting site validation activities to ensure equipment and process compliance at Bausch + Lomb's Greenville, SC facility. Responsibilities: lead and coordinate re-qualifications of sterilizers, aseptic systems, and process validations; author validation strategies and protocols; analyze validation data; write final reports; perform periodic reviews and peer assessments of validation packages; support validation projects related to equipment and process changes. Requirements: Associate Degree in Science (BS preferred); 0-3 years validation experience, with up to 5 years in pharma/medical device manufacturing or QC labs; experience with Ellab data loggers or equivalents; strong GMP knowledge, data integrity, and communication skills; results-oriented with a quality mindset. High-Value: validation of sterilization, aseptic processes, media fills, and cleaning processes within a pharmaceutical and medical device manufacturing environment. WorkSetup: Greenville, SC, potential on-site work.