Validation Engineer

  • Company:
    PSC Biotech
  • Location:
  • Salary:
    negotiable / month
  • Job type:
    Full-Time
  • Posted:
    14 hours ago
  • Category:
    Pharmaceuticals

PSC Biotech is a leading Biotech Consultancy firm founded in 1996, headquartered in Pomona, California, employing a global team of skilled professional and experts that span across strategically located offices in the United States, Europe, Asia, and the Middle East. PSC operates in 52 countries globally and has served thousands of clients to date. We focus on providing quality consulting services to ensure our clients success. PSC provides cost-effective solutions, while providing exceptional technical capabilities and customer service to our clients for all projects ranging from supplier quality audits to greenfield projects. We understand that the world of life science is evolving rapidly, and we must continue to offer new products and services to meet our customers expectations. We are looking for a Validation Engineer to join our team. The candidate must have experience in both equipmentvalidationand cleaning validation. Responsibilities Responsible for Equipment Validation for tank, new filler (IOQ), and cleaning validation Write, Edit, and Execute IQ and OQ Develop validation master plans with minimum supervision Prepare protocols independently Analyze test results Prepare all technical reports Responsible for coordination and execution of validation activities in accordance with current Good Manufacturing Practices (GMPs) Execute and support all cleaning validation activities Generate reference documents and cleaning SOPs based on cleaning cycles Other duties as assigned Requirements 8+ years of related experience Strong background and experience in Equipment Validation Strong background in Cleaning Validation Knowledge of Installation Qualification, Operational Qualification, and Performance Qualification Demonstrated strong communication skills (written and verbal) Experience executing validation protocols i Strong Knowledge of GMP regulations Excellent Technical Writing skills