Job Details

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

...@dawarconsulting.com/...@dawarconsulting.com