Validation Engineer

BEPC is actively looking for Validation Engineer, in Tucson, AZ area!

W2 Contract – 12 months with possible extensions!

Benefits include medical, dental, vision, and life insurance

Pay Rate: $39.00 - $42.00 /hour - Determined based on experience (Paid weekly)

Work Model:
Onsite role

Note
:
This is a W2 only role — C2C, C2H will not be considered

BEPC is seeking a highly motivated Validation Engineer to join our client’s site in Tucson, AZ. This role will support process validation activities in a regulated manufacturing environment to ensure compliance and drive operational integrity.

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) to ensure compliance and drive operational integrity.

• Develop, write, review, and execute process validation/process verification protocols and reports.
• Conduct risk assessments and develop validation strategies for new and existing processes.
• Analyze and interpret process validation data, ensuring accuracy, completeness, and adherence to regulatory and internal requirements.
• Collaborate with Manufacturing, Quality, Design Transfer Operations, and other departments 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, and other relevant regulatory guidelines, as well as adherence to internal requirements.
• Provide training and guidance to manufacturing and quality personnel on validation processes and procedures.
• Maintain process validation documentation and ensure traceability and accessibility for audits and inspections.
• Other duties as assigned by management.

• Education:
  
  Bachelor’s Degree in Engineering or Life Science.
• Strong technical writing, analytical, and problem-solving skills.
• Knowledge of cGMP and regulatory standards.
• Strong understanding of process validation principles, techniques, and industry standards.

• 1-3 years of experience in a regulated manufacturing environment (medical devices, pharma, or biotech, preferably FDA).