Job Description
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
hr@dawarconsulting.com / saurav@dawarconsulting.com