Validation Engineer

Job Description
Our client, a world leader in biotechnology and life sciences, is looking for a " Validation Engineer " based out in Tucson, AZ.


Job Duration: Long Term Contract (Possibility Of Extension & FT Conversion)

Rate: $39-$42/hr on W2

Company Benefits: Medical, Dental, Vision, Paid Sick leave, 401K

Job Summary:

We are seeking a proactive Validation Engineer with 1-3 years of experience in a regulated manufacturing environment such as medical devices, pharmaceuticals, or biotechnology. This on-site role focuses on process validation activities to ensure compliance with FDA, ISO, cGMP, and internal quality standards while supporting continuous improvement and operational excellence.

Key Responsibilities:

• Develop, write, review, and execute process validation and process verification protocols and reports
• Conduct risk assessments and support validation strategies for new and existing manufacturing processes
• Analyze and interpret validation data to ensure compliance with regulatory and internal quality requirements
• Collaborate with Manufacturing, Quality, and Design Transfer teams to resolve validation issues and implement corrective actions
• Support process optimization and continuous improvement initiatives to improve quality and efficiency
• Ensure compliance with FDA, ISO, cGMP, and internal regulatory standards
• Maintain validation documentation, traceability records, and audit-ready files
• Provide training and guidance on validation processes, procedures, and compliance requirements

Required Qualifications:

• Bachelor's degree in Engineering, Life Sciences, or related field
• 1-3 years of experience in validation within a regulated manufacturing environment
• Knowledge of process validation principles, verification techniques, and industry standards
• Familiarity with FDA regulations, ISO standards, and cGMP requirements
• Strong technical writing, analytical, and problem-solving skills
• Excellent communication and cross-functional collaboration abilities

Preferred Experience:

• Medical device, biotech, or pharmaceutical industry experience
• Experience supporting audits, CAPA activities, and process improvement initiatives
• Familiarity with risk assessments and validation documentation practices

Key Skills:

Process ValidationProcess VerificationFDA CompliancecGMPISO StandardsValidation ProtocolsRisk AssessmentsCAPATechnical WritingRoot Cause AnalysisQuality SystemsContinuous ImprovementManufacturing ValidationRegulatory Compliance

If interested, please send us your updated resume at View email address on click.appcast.io/View email address on click.appcast.io.

Skill Set
Process Validation, Process Verification, FDA