Validation Analyst/Senior Validation Analyst, Clinical Research

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale.

Join the PPD™ clinical research business of Thermo Fisher Scientific, where our mission is to enable our customers to make the world healthier, cleaner, and safer. We partner with leading pharmaceutical, biotechnology, medical device, academic, and government organizations to accelerate the development of life-changing therapies.

As part of our Global Digital & Technology organization, you'll help ensure the quality and compliance of technology solutions that support clinical research worldwide. Your work directly contributes to patient safety, regulatory compliance, and the successful delivery of innovative medicines.

Discover Impactful Work
As a Senior Validation Analyst, you will play a critical role in the entire product development lifecycle by validating regulated computer systems used across the clinical research organization. You will partner with cross-functional teams to ensure software applications and digital/AI products meet regulatory requirements, business needs, and quality standards throughout the system development lifecycle (SDLC).

You'll lead validation activities for new digital implementations, enhancements, and upgrades while supporting compliance with GxP regulations, company SOPs, and industry best practices. Familiarity with risk-based validation methodologies is a plus!

A Day in the Life

• Lead computerized system validation (CSV) activities for regulated digital and AI applications throughout the SDLC. 
• Develop and execute validation deliverables including Validation Plans, Risk Assessments, IQ/OQ/PQ documentation (where applicable), test scripts, traceability matrices, and Validation Summary Reports. 
• Partner with Business Analysts, Quality Assurance, IT, vendors, and project teams to ensure systems meet business and regulatory requirements. 
• Review software requirements, functional specifications, design documentation, and change controls to ensure validation readiness. 
• Design, execute, and document risk-based testing strategies that demonstrate systems perform as intended. 
• Create and maintain validation evidence in accordance with internal procedures and regulatory expectations. 
• Support system implementations, upgrades, patches, and application enhancements. 
• Review and approve validation-related change controls and ensure ongoing compliance for validated systems. 
• Investigate test failures, identify root causes, and collaborate with technical teams to resolve issues. 
• Participate in internal audits, sponsor audits, and regulatory inspections by providing validation documentation and subject matter expertise. 
• Contribute to continuous improvement initiatives that enhance validation processes, testing efficiency, and compliance. 

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Keys to Success
Education

• Bachelor's degree in Computer Science, Information Systems, Life Sciences, Engineering, or a related discipline; or equivalent and relevant formal academic / vocational qualification.

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Experience

• 5-8 years of experience in computerized system validation, software quality, or validation within a regulated environment. 
• Experience supporting GxP-regulated systems in the pharmaceutical, biotechnology, CRO, medical device, or healthcare industries highly preferred. 
• Experience working within Software Development Life Cycle (SDLC) methodologies. 
• Experience supporting validation of enterprise applications, SaaS platforms, or commercial off-the-shelf (COTS) software preferred. 
• Experience with change management and validation documentation in regulated environments. 

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Preferred Qualifications

• Experience validating cloud-based or SaaS applications. 
• Experience with Jira, Azure DevOps, HP ALM, or similar tools. 
• Experience supporting clinical trial systems (CTMS, eTMF, EDC, LIMS, Safety, ERP, or Laboratory systems). 
• Knowledge of computerized system lifecycle documentation and risk assessments. 
• Experience participating in regulatory inspections or customer audits. 

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Knowledge, Skills, Abilities

• Strong understanding of Computerized System Validation (CSV) principles. 
• Knowledge of FDA 21 CFR Part 11, GAMP 5, GxP, ALCOA+ principles, and applicable regulatory guidance.