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

hr@dawarconsulting.com
/saurav
@dawarconsulting.com