College Station, TX1 day ago
Qualifications: Master's Degree in Engineering Discipline or Science Discipline and 3+ years of direct Validation experience in pharmaceutical, biotechnology, or related industry, preferably in FDA-regulated environment, OR; Bachelor's Degree and 5+ years of direct Validation experience in pharmaceutical, biotechnology, or related industry, preferably in FDA-regulated environment. Primary Responsibilities: Generate VPPs, SIAs, obtain approvals and execute validation deliverables for FUSE systems and relevant infrastructure, including, Risk Assessments, Installation/Operational Qualifications and Performance Qualifications (as applicable) and Validation Final Reports, ensuring documents meet regulatory and procedural requirements.