Validation Engineer

Dawar Consulting

Tucson, Arizona

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JOB DETAILS

SKILLS

Analysis Skills, Biology, Biotech and Pharmaceutical, Communication Skills, Continuous Improvement, Corrective Action, Corrective and Preventative Action (CAPA) Systems, Cross-Functional, Current Good Manufacturing Practice (cGMP), FDA (Food and Drug Administration), FDA Requirements, File Audits, ISO (International Organization for Standardization), Industry Standards, Maintain Compliance, Manufacturing, Manufacturing/Industrial Processes, Medical Equipment, Operational Improvement, Problem Solving Skills, Process Improvement, Process Validation, Quality Assurance, Quality Management, Quality Metrics, Regulatory Compliance, Risk Analysis, Root Cause Analysis, Team Player, Technical Writing, Traceability, Training/Teaching, Validation Documentation, Validation Plan, Validation Testing, Writing Skills

LOCATION

Tucson, Arizona

POSTED

1 day ago

Our client, a world leader in biotechnology and life sciences, is looking for a “Validation Engineer<\/b>" based out in Tucson, AZ.
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Job Duration:<\/b> Long Term Contract (Possibility Of Extension & FT Conversion)
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Rate:<\/b> $39 -$42/hr on W2
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Company Benefits:<\/b> Medical, Dental, Vision, Paid Sick leave, 401K
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Job Summary:<\/b>
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We are seeking a proactive <\/span>Validation Engineer<\/b> <\/span>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.
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Key Responsibilities:<\/b>
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Develop, write, review, and execute process validation and process verification protocols and reports
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Conduct risk assessments and support validation strategies for new and existing manufacturing processes
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Analyze and interpret validation data to ensure compliance with regulatory and internal quality requirements
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Collaborate with Manufacturing, Quality, and Design Transfer teams to resolve validation issues and implement corrective actions
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Support process optimization and continuous improvement initiatives to improve quality and efficiency
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Ensure compliance with FDA, ISO, cGMP, and internal regulatory standards
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Maintain validation documentation, traceability records, and audit -ready files
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Provide training and guidance on validation processes, procedures, and compliance requirements
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Required Qualifications:<\/b>
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Bachelor’s degree in Engineering, Life Sciences, or related field
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1–3 years of experience in validation within a regulated manufacturing environment
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Knowledge of process validation principles, verification techniques, and industry standards
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Familiarity with FDA regulations, ISO standards, and cGMP requirements
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Strong technical writing, analytical, and problem -solving skills
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Excellent communication and cross -functional collaboration abilities
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Preferred Experience:<\/b>
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Medical device, biotech, or pharmaceutical industry experience
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Experience supporting audits, CAPA activities, and process improvement initiatives
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Familiarity with risk assessments and validation documentation practices
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Key Skills:<\/b>
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Process Validation | Process Verification | FDA Compliance | cGMP | ISO Standards | Validation Protocols | Risk Assessments | CAPA | Technical Writing | Root Cause Analysis | Quality Systems | Continuous Improvement | Manufacturing Validation | Regulatory Compliance
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If interested, please send us your updated resume at
hr@dawarconsulting.com
kavitha@dawarcosnulting.com

Validation Engineer

Dawar Consulting

Tucson, Arizona

About the Company

Dawar Consulting

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