Validation Engineer

Validation Engineer

Tucson, United States

Long Term Contract (Possibility Of Extension & FT Conversion)

$39-$42/hr on W2

Medical, Dental, Vision, Paid Sick leave, 401K

We are seeking a proactive Validation Engineer with 1–3 years of experience in a regulated manufacturing environment such as medical devices, pharmaceuticals, or biotechnology. This on-site role focuses on process validation activities to ensure compliance with FDA, ISO, cGMP, and internal quality standards while supporting continuous improvement and operational excellence.

• Develop, write, review, and execute process validation and process verification protocols and reports
• Conduct risk assessments and support validation strategies for new and existing manufacturing processes
• Analyze and interpret validation data to ensure compliance with regulatory and internal quality requirements
• Collaborate with Manufacturing, Quality, and Design Transfer teams to resolve validation issues and implement corrective actions
• Support process optimization and continuous improvement initiatives to improve quality and efficiency
• Ensure compliance with FDA, ISO, cGMP, and internal regulatory standards
• Maintain validation documentation, traceability records, and audit-ready files
• Provide training and guidance on validation processes, procedures, and compliance requirements

• Bachelor’s degree in Engineering, Life Sciences, or related field
• 1–3 years of experience in validation within a regulated manufacturing environment
• Knowledge of process validation principles, verification techniques, and industry standards
• Familiarity with FDA regulations, ISO standards, and cGMP requirements
• Strong technical writing, analytical, and problem-solving skills
• Excellent communication and cross-functional collaboration abilities

• Medical device, biotech, or pharmaceutical industry experience
• Experience supporting audits, CAPA activities, and process improvement initiatives
• Familiarity with risk assessments and validation documentation practices

• Process Validation
• Process Verification
• FDA Compliance
• cGMP
• ISO Standards
• Validation Protocols
• Risk Assessments
• CAPA
• Technical Writing
• Root Cause Analysis
• Quality Systems
• Continuous Improvement
• Manufacturing Validation
• Regulatory Compliance

Process Validation, Process Verification, FDA