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Manager Work From Home Computer System Validation Csv Jobs

Tempus

Senior Quality Engineer

Chicago, IL · On-site +1

Lead computer system validation (CSV) activities of Tempus AI applications, software tools, and ... Support Change Management and Major Incidents (MI) processes, ensuring organizational compliance ...

Tempus

Senior Quality Engineer

New York, NY · On-site +1

Lead computer system validation (CSV) activities of Tempus AI applications, software tools, and ... Support Change Management and Major Incidents (MI) processes, ensuring organizational compliance ...

Tempus

Senior Quality Engineer

Redwood City, CA · On-site +1

Lead computer system validation (CSV) activities of Tempus AI applications, software tools, and ... Support Change Management and Major Incidents (MI) processes, ensuring organizational compliance ...

Vaxcyte

Manager, IT Quality & Compliance

San Carlos, CA · On-site +1

IT Validation & CSV/CSA Execution * Execute Computer Software Assurance (CSA) and Computer System ... Author and maintain IT and QA SOPs, policies, and work instructions. * Ensure alignment with GxP ...

CREO

Senior Analyst - GxP IT QA/CSV

Durham, NC · On-site +1

This includes Computer Systems Validation (CSV) and, importantly, applying modern approaches to ... Manage and communicate complex IT compliance concepts to both technical and non-technical audiences ...

CREO

Senior Analyst - GxP IT QA/CSV

Durham, NC · Remote

This includes Computer Systems Validation (CSV) and, importantly, applying modern approaches to ... Manage and communicate complex IT compliance concepts to both technical and non-technical audiences ...

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How much do manager work from home computer system validation csv jobs pay per year?

As of Jun 8, 2026, the average yearly pay for manager work from home computer system validation csv in the United States is $105,415.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,500.00 and $132,000.00 per year, depending on experience, location, and employer.

What is the difference between Manager Work From Home Computer System Validation Csv vs Computer System Validation Specialist?

AspectManager Work From Home Computer System Validation CsvComputer System Validation Specialist
CredentialsTypically requires a bachelor's degree in life sciences, IT, or related field; certifications like GxP, CSV certifications are commonRequires similar degrees and certifications, often focusing on CSV-specific credentials
Work EnvironmentRemote work, overseeing validation projects, managing teams, and ensuring compliancePrimarily on-site or hybrid, executing validation tasks and documentation
Industry UsageUsed in regulated industries like pharmaceuticals, biotech, and healthcareCommonly employed in similar regulated environments for validation activities

While both roles require similar credentials and industry knowledge, the Manager Work From Home Computer System Validation Csv focuses on overseeing validation projects remotely, managing teams, and ensuring compliance, whereas the Computer System Validation Specialist typically performs hands-on validation tasks on-site or in hybrid settings.

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Manager Work From Home Computer System Validation Csv jobs near you
Manager, Quality Computerized System Validation (CSV)

Manager, Quality Computerized System Validation (CSV)

Nuvalent, Inc.

Cambridge, MA • Remote

Other

Posted 20 days ago

Job description

The Role:

Reporting to the Director, Quality Systems, the Manager, Quality Computerized System Validation (CSV) is responsible for maintaining the validation lifecycle of GxP-regulated computerized systems across the organization in a remote pharmaceutical operating model. The ideal candidate is a strategic thinker with strong hands-on validation experience, excellent cross-functional communication skills, and understanding of compliance in a cloud-based and SaaS environment.

Responsibilities:

  • Partner with IT, Quality, Regulatory, Clinical, TechOps, Pharmacovigilance, and vendors to support GxP system implementations, enhancements, and upgrades.
  • Develop, maintain, and continuously improve CSV policies, SOPs, and forms aligned with regulatory expectations and industry best practices.
  • Ensure application of risk-based validation approaches and data integrity principles (ALCOA++).
  • Act as CSV subject during internal audits, vendor audits, and regulatory inspections.
  • Review and approve GxP system validation deliverables, change controls, deviation investigations, and periodic reviews.
  • Assess inspection trends and proactively update validation practices accordingly.
  • Evaluate vendor documentation for GxP system validation and SDLC for suitability and leverage where appropriate.

 Competencies:

  • Risk-based decision making
  • Strategic thinking with practical execution
  • Strong written and verbal communication
  • Attention to detail with business mindset

 Qualifications:

  • Bachelor's degree or related experience
  • 3-5 years' experience in GxP computerized system validation within the pharmaceutical, biotech, or medical device industry.
  • Veeva QualityDocs experience required.
  • Deep knowledge of CSV, SDLC, Part 11, Annex 11, ICH E6(R3) Data Governance, and data integrity principles.
  • Experience validating cloud-based and SaaS systems.
  • Strong understanding of change management and system lifecycle management.
  • Ability to work Eastern Time Zone and across time zones as needed 

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