Validation Engineer

Our client, a world leader in diagnostics and life sciences, is looking for a "Validation Engineer” based out of Tucson, AZ 

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.
  

• 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

/saurav