Cognizant

Veeva Vault RIM Test & Validation Lead (CSV / QEA)

Cognizant$71K — $112K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • 3-5 years of hands-on experience with Veeva Vault RIM (configuration and support)
  • 8+ years of experience in Computer System Validation (CSV), including protocol development
  • Proven experience in the Life Sciences industry 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 to ensure compliance with GxP standards
  • Develop and execute validation strategies, including risk assessments and test planning
  • Author and review validation documentation like validation plans and test scripts
  • Oversee test execution, defect management, and resolution with cross-functional teams
  • Manage change control and end-to-end validation lifecycle for regulatory systems

Benefits

  • Medical/Dental/Vision/Life Insurance
  • Paid holidays plus Paid Time Off
  • 401(k) plan and contributions
  • Long-term/Short-term Disability
  • Paid Parental Leave
  • Employee Stock Purchase Plan
Full Job Description
About the role

As a Veeva Vault RIM Test & Validation Lead (CSV / QEA), you will make an impact by driving validation strategy and ensuring compliance of regulatory systems supporting global submissions. You will be a valued member of the regulatory technology team and work collaboratively with regulatory affairs, quality, and IT stakeholders.

In this role, you will:

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 in collaboration with cross-functional teams

Manage change control, demand prioritization, and end-to-end validation lifecycle for regulatory systems

Work model

We believe hybrid work is the way forward as we strive to provide flexibility wherever possible. Based on this role's business requirements, this is a hybrid position requiring 2-3 days a week in a client or Cognizant office in Boston, MA.

The working arrangements for this role are accurate as of the date of posting. This may change based on the project you're engaged in, as well as business and client requirements. Rest assured; we will always be clear about role expectations.

What you need to have to be considered

3-5 years of hands-on experience with Veeva Vault RIM (configuration and support)

8+ years of strong experience in Computer System Validation (CSV), including protocol development and compliance

Proven experience in the Life Sciences industry 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

These will help you stand out

Exposure to AI assurance or validation of AI-enabled systems

Experience estimating testing efforts and planning validation activities across projects

Strong understanding of risk-based validation strategies

Ability to prioritize work based on regulatory impact and business criticality

Experience working in cross-functional or global delivery environments

We're excited to meet people who share our mission and can make an impact in a variety of ways. Don't hesitate to apply, even if you only meet the minimum requirements listed. Think about your transferable experiences and unique skills that make you stand out as someone who can bring new and innovative ideas to this role.

Salary and Other Compensation

The annual salary for this position is between $71,100 to $112,500, depending on experience and other qualifications of the successful candidate.

This position is also eligible for Cognizant's discretionary annual incentive program, based on performance and subject to the terms of Cognizant's applicable plans.

Benefits:

Cognizant offers the following benefits for this position, subject to applicable eligibility requirements:

Medical/Dental/Vision/Life Insurance

Paid holidays plus Paid Time Off

401(k) plan and contributions

Long-term/Short-term Disability

Paid Parental Leave

Employee Stock Purchase Plan

About Cognizant

TriZetto is Powering Integrated Healthcare Management. With technology solutions touching more than half the U.S. population today, TriZetto is uniquely positioned to drive the convergence of core benefit administration, care management and constituent engagement. TriZetto provides premier information technology solutions that enable payers and other constituents in the healthcare supply chain to improve the coordination of benefits and care for healthcare consumers.

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Learn more about Cognizant
Size
340,400 employees
Market Cap
$28.7 billion
Industry
Net Income
$1.3 billion
Founded
1994
5 Year Trend
+6.5%
Revenue
$16.6 billion
NASDAQ

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