Validation Engineer

Job Description Our client, a world leader in diagnostics and life sciences, is looking for a "Validation Engineer" based out of Tucson, AZ Job Title: Validation Engineer Location: On-site Tucson, AZ Experience Required: 1-3 years We are seeking a proactive Validation Engineer with 1-3 years of experience in a regulated manufacturing environment (medical devices, pharma, or biotech, preferably FDA-regulated). The role focuses on process validation to ensure compliance and drive operational integrity. Key Responsibilities Develop, write, review, and execute process validation and verification protocols and reports. Conduct risk assessments and develop validation strategies for new and existing processes. Analyze and interpret validation data to ensure accuracy, completeness, and compliance with regulatory and internal requirements. Collaborate with Manufacturing, Quality, Design Transfer Operations, and other teams to resolve validation issues and implement corrective actions. Participate in process optimization and continuous improvement initiatives to enhance quality and efficiency. Ensure compliance with FDA, ISO, cGMP, and other relevant regulatory guidelines. Provide training and guidance to manufacturing and quality personnel on validation processes and procedures. Maintain process validation documentation to ensure traceability and readiness for audits and inspections. Perform other duties as assigned by management. Qualifications Bachelor's Degree in Engineering or Life Sciences. Strong technical writing, analytical, and problem-solving skills. Knowledge of cGMP and regulatory standards. Solid understanding of process validation principles, techniques, and industry standards. Company Benefits: Medical, Dental, Vision, Paid Sick leave, 401K If interested, please send us your updated resume at /

Created: 2026-03-10