Validation Lead

Summary The Validation Lead is responsible for leading end-to-end validation activities within a regulated pharmaceutical, biotechnology, medical device, or life sciences environment. The role develops validation strategies, coordinates cross-functional teams, oversees qualification and validation execution, and ensures compliance with GMP/GxP, FDA requirements, GAMP 5, and data integrity expectations. Typical responsibilities include process, equipment, facility/utilities, cleaning, and/or computerized system validation depending on the program. Responsibilities Lead and coordinate validation activities from planning through final approval. Develop and maintain Validation Master Plans (VMPs) and project-specific validation strategies. Prepare, review, and approve validation documents including URS, risk assessments, DQ, IQ, OQ, PQ, traceability matrices, protocols, and validation summary reports. Lead process, equipment, cleaning, facility/utilities, and/or computerized system validation activities as applicable. Coordinate validation execution with Quality, Engineering, Manufacturing, Automation, IT, Laboratory, and external vendors. Manage deviations, discrepancies, CAPAs, and change controls associated with validation activities. Ensure validation deliverables meet project timelines and regulatory requirements. Provide technical leadership for validation investigations and complex validation challenges. Monitor validation metrics, project progress, risks, and issues. Support audits, regulatory inspections, inspection readiness, product launches, and technical transfers. Provide technical guidance and mentoring to validation engineers and specialists. Identify opportunities to improve validation processes, documentation, and execution efficiency. Requirements Bachelor's degree in Engineering, Chemistry, Pharmacy, Life Sciences, Biotechnology, Pharmaceutical Sciences, or a related technical discipline. Typically 5+ years of validation experience, with lead-level roles often requiring substantially more experience depending on scope. Strong experience in a GMP/GxP-regulated pharmaceutical, biotech, medical device, or life sciences environment. Hands-on knowledge of the validation lifecycle, including URS, risk assessment, IQ/OQ/PQ, traceability, and validation reports. Strong knowledge of FDA regulations, cGMP, GAMP 5, 21 CFR Part 11, EU Annex 11, and data integrity principles where applicable. Experience leading cross-functional validation projects and managing multiple priorities. Strong technical writing, documentation, communication, and stakeholder-management skills. Experience with deviations, CAPA, change control, and quality systems. Ability to support audits and regulatory inspections. Strong analytical, troubleshooting, organizational, and problem-solving skills. Experience with validation management/documentation tools such as Kneat, ValGenesis, TrackWise, Veeva, or similar platforms is beneficial. #J-18808-Ljbffr Katalyst CRO