Hybrid Veeva Vault RIM Validation Lead (CSV/QA)

Cognizant; Annapolis (MD); Hybrid; USD 71,000 - 113,000; Full time

Benefits offered by this job

Medical Insurance

Dental Insurance

Vision Insurance

Life Insurance

Paid Holidays

Paid Time Off

401(k) Plan

Disability Insurance

Parental Leave

Employee Stock Purchase Plan

Job summary

Cognizant is seeking a Veeva Vault RIM Test & Validation Lead (CSV / QEA) to drive validation strategy and ensure regulatory compliance for global submissions. You will collaborate with regulatory affairs, quality, and IT to lead validation activities for Veeva Vault RIM and manage end-to-end lifecycle.

The role requires 8+ years in CSV with GxP exposure and experience in the Life Sciences industry, plus strong risk-based validation skills.

Qualifications

• 3-5 years hands-on experience with Veeva Vault RIM (configuration and support)
• 8+ years of strong experience in Computer System Validation (CSV) including protocol development
• Proven experience in Life Sciences with knowledge of GxP requirements
• Understanding of Regulatory Affairs and global submission standards (e.g., eCTD)
• Experience with regulatory submission processes and health authority interactions

Responsibilities

• Lead validation activities for Veeva Vault RIM ensuring compliance with GxP and regulatory standards
• Develop and execute validation strategies including risk assessments, test planning, and protocol development
• Author and review validation documentation such as validation plans, test scripts, traceability matrices, and reports
• Oversee test execution, defect management, and resolution with cross-functional teams
• Manage change control and end-to-end validation lifecycle for regulatory systems

Skills

Veeva Vault RIM

CSV Validation

Regulatory Affairs

GxP Knowledge

Cross-functional Collaboration

Job description

Cognizant is seeking a Veeva Vault RIM Test & Validation Lead (CSV / QEA) to drive validation strategy and ensure regulatory compliance for global submissions. You will collaborate with regulatory affairs, quality, and IT to lead validation activities for Veeva Vault RIM and manage end-to-end lifecycle.

The role requires 8+ years in CSV with GxP exposure and experience in the Life Sciences industry, plus strong risk-based validation skills.