Senior CSV Analyst

Senior Computer System Validation Analyst

We are seeking an experienced Senior Computer System Validation (CSV) Analyst to support validation and compliance activities for GxP computerized systems in a regulated pharmaceutical/biotechnology environment. The ideal candidate will have strong knowledge of GAMP 5, 21 CFR Part 11, EU Annex 11, risk-based validation, and Computer Software Assurance (CSA) principles.

Responsibilities include:

• Leading and executing Computer System Validation (CSV) activities throughout the system lifecycle.
• Developing and maintaining Validation Plans, User Requirements Specifications (URS), Functional Specifications (FS), Risk Assessments, test protocols, and validation reports.
• Executing and documenting IQ/OQ/PQ, UAT, regression, and risk-based testing as applicable.
• Ensuring computerized systems remain in a validated state throughout their lifecycle.
• Performing GxP impact assessments, validation risk assessments, and system categorization.
• Applying GAMP 5 and CSA principles to validation strategies and testing approaches.
• Supporting 21 CFR Part 11 and EU Annex 11 compliance assessments.
• Reviewing system requirements, specifications, test scripts, and traceability matrices.
• Supporting Change Control, Deviation, CAPA, and Periodic Review activities.
• Reviewing and assessing audit trails, user access, electronic records, and electronic signatures.
• Supporting internal audits and FDA/regulatory inspection readiness.
• Collaborating with IT, Quality Assurance, Business Process Owners, System Owners, and vendors.
• Identifying validation gaps and developing appropriate remediation strategies.
• Ensuring validation documentation is accurate, complete, traceable, and inspection-ready.
• Supporting system upgrades, implementations, migrations, and integrations.
• Providing technical guidance and mentoring to junior CSV team members.

Requirements include:

• Bachelor's degree in Computer Science, Information Technology, Engineering, Life Sciences, Pharmacy, or a related field.
• 5–8+ years of experience in Computer System Validation, Quality Systems, or GxP IT environments.
• Strong experience validating GxP computerized systems in pharmaceutical, biotechnology, medical device, or other regulated industries.
• Hands-on experience with GAMP 5, 21 CFR Part 11, EU Annex 11, and CSA.
• Experience with enterprise GxP applications such as Veeva, SAP, LIMS, MES, QMS, ERP, or clinical systems is preferred.
• Strong technical writing, analytical, problem-solving, and communication skills.
• Ability to manage multiple validation projects and priorities in a regulated environment.