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.
This is an on-site position that focuses on equipment validation.
Responsibilities:
Develops, prepares, and executes IQ, OQ, and PQ protocols and reports for equipment/systems.
Conducts risk assessments and develops qualification strategies for new and existing equipment/systems.
Analyzes and interprets qualification data, ensuring accuracy, completeness, and adherence to regulatory and internal requirements.
Collaborates with cross-functional teams, including Process Engineering, Automation Maintenance Support, Design Transfer Operations, Manufacturing, Quality, Facilities, and Safety Health and Environment (SHE), to ensure seamless execution of qualification activities and successful achievement of qualification-related project milestones.
Participates in process optimization and continuous improvement initiatives to enhance quality and efficiency.
Ensures compliance with FDA, ISO, and other relevant regulatory guidelines, as well as adherence to internal requirements.
Provides training and guidance to manufacturing and quality personnel on qualification processes and procedures.
Maintains equipment/systems qualification documentation and ensures traceability and accessibility for audits and inspections.
Other duties as assigned by management.
Requirements:
Bachelor's degree in engineering or Life Science.
Strong technical writing, analytical, and problem-solving skills.
Knowledge of cGMP and regulatory standards.
Demonstrated experience assisting with or supporting qualification activities within the medical device, pharmaceutical, or biotechnology industry is required.
Experience: 1-3 years of experience in a regulated manufacturing environment (medical devices, pharma, or biotech, preferably FDA).
Numbers & Facts
Location
Tucson, AZ
Skills
Analysis Skillsunmatched
Automationunmatched
Biologyunmatched
Biotech and Pharmaceuticalunmatched
Continuous Improvementunmatched
Cross-Functionalunmatched
Current Good Manufacturing Practice (cGMP)unmatched
Documentationunmatched
Equipment Maintenance/Repairunmatched
Equipment Validationunmatched
FDA (Food and Drug Administration)unmatched
ISO (International Organization for Standardization)unmatched
Maintain Complianceunmatched
Manufacturingunmatched
Medical Equipmentunmatched
Problem Solving Skillsunmatched
Process Engineeringunmatched
Process Improvementunmatched
Process Validationunmatched
Quality Assuranceunmatched
Regulationsunmatched
Regulatory Complianceunmatched
Risk Analysisunmatched
Safety/Work Safetyunmatched
Strategic Planningunmatched
Systems Maintenanceunmatched
Technical Writingunmatched
Traceabilityunmatched
Training/Teachingunmatched
Writing Skillsunmatched
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