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Manager Work From Home Computer System Validation Csv Jobs

Tempus

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 ...

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 ...

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Manager Work From Home Computer System Validation Csv information

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$47.5K

$105.4K

$160.5K

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

As of Jul 21, 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.

What cities are hiring for Manager Work From Home Computer System Validation Csv jobs? Cities with the most Manager Work From Home Computer System Validation Csv job openings:
What states have the most Manager Work From Home Computer System Validation Csv jobs? States with the most job openings for Manager Work From Home Computer System Validation Csv jobs include:
What job categories do people searching Manager Work From Home Computer System Validation Csv jobs look for? The top searched job categories for Manager Work From Home Computer System Validation Csv jobs are:
Manager Work From Home Computer System Validation Csv jobs near you
Infographic showing various Manager Work From Home Computer System Validation Csv job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 75% Full Time, 13% Part Time, and 11% Contract. Highlights an 85% Physical, 2% Hybrid, and 13% Remote job distribution, with an average salary of $105,415 per year, or $50.7 per hour.

Validation Consultant - Computer System Validation (CSV/CSA)

Pine Services Group

Remote

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 7 days ago

Job description

One of Pine's portfolio companies is a leading consulting firm specializing in ERP, quality management, and manufacturing solutions for life science manufacturers. They implement QAD Adaptive ERP, QAD EQMS, NetSuite, ETQ QMS, and related technologies - helping clients navigate clinical-to-commercial transitions, regulatory compliance, and operational excellence. They're looking for a Validation Consultant to serve as a senior technical authority for computer system validation (CSV) and computer software assurance (CSA) across their life science consulting portfolio.
The successful candidate will establish and maintain the firm's validation strategy, extend its validation toolkits across QAD, NetSuite, QAD EQMS, ETQ, and supporting add-on platforms, and lead end-to-end validation delivery on client engagements. This role works alongside the current Validation Practice Lead and is accountable for ensuring every validation package produced is inspection-ready and aligned with cGxP, GAMP 5 Category 4, CSA, EU Annex 11, 21 CFR Part 11, and data integrity expectations.
This is a full-time primarily role with approximately 10% travel to client sites, primarily within North America.
What You'll Do
  • Establish and maintain the firm's validation strategy and standards, ensuring all deliverables align with cGxP, GAMP 5 Category 4, CSA, EU Annex 11, 21 CFR Part 11, and ALCOA+ data integrity principles.
  • Maintain and continuously improve validation toolkits for QAD ERP, NetSuite, QAD EQMS, and ETQ - including URS/FRS templates, risk assessments, requirements traceability matrices (RTMs), IQ/OQ/PQ scripts, and script libraries.
  • Maintain standalone validation toolkits for Serialization, Automated Solutions, ISS-Group (iApprove/iPurchase), and Eagle RF.
  • Analyze software release specifications and release notes to determine validation impact, risk, and required deliverable updates.
  • Build new validation toolkit frameworks for new software platforms and modules as the service portfolio expands.
  • Lead end-to-end client validation engagements, including validation planning, protocol authoring, execution support, evidence review, deviation handling, and validation summary reporting (VSR).
  • Provide validation guidance and execution support to client teams as embedded staff augmentation.
  • Interpret client SOPs and internal CSV/QMS requirements, tailoring deliverables to meet both client-internal and regulatory expectations.
  • Mentor junior validation consultants and contribute to the firm's Computer Validation as a Service (CVaaS) offering.

What They're Looking For
Required
  • 10+ years of experience in computer system validation (CSV) or computer software assurance (CSA) for life science manufacturers.
  • Deep working knowledge of cGxP, GAMP 5 Category 4, 21 CFR Part 11, EU Annex 11, ALCOA+, and CSA principles applied to risk-based validation.
  • Familiarity with 21 CFR Part 820/QMSR and ISO 13485 quality system requirements.
  • Demonstrated ability to design and maintain reusable validation toolkits, including URS/FRS templates, RTMs, IQ/OQ/PQ scripts, risk assessments, and validation summary reports.
  • Strong release impact analysis skills - able to translate software release specifications into validation scope, risk, and deliverable updates.
  • Excellent technical and compliance writing skills, producing audit-ready validation documentation.
  • Experience executing or supporting validation protocol execution, including evidence capture, deviation documentation, and results review.
  • Proven client stakeholder communication skills across QA, IT, and business functions.
  • Experience operating as staff augmentation, integrating into client teams and working within client QMS and SDLC constraints.
  • Bachelor's degree in Engineering, Life Sciences, Computer Science, or a related field; advanced degree a plus.

Nice to Have
  • Hands-on validation experience with QAD ERP, NetSuite, QAD EQMS, or ETQ.
  • Hands-on validation experience with QAD add-ons including Serialization, Automated Solutions, ISS-Group (iApprove/iPurchase), and Eagle RF.
  • Experience building net-new validation toolkit frameworks for emerging software offerings.
  • Experience supporting CSV/CSA programs for medical device or pharmaceutical manufacturers.
  • Validation-related professional certifications (ASQ CQA and/or CQE).
  • Prior consulting experience in a continuous release validation process or managed validation services model.

What They Offer
  • Location: Remote (US)
  • Employment Type: Full-Time
  • Travel: Approximately 10%, primarily within North America
  • Benefits: Competitive benefits package (medical, dental, vision), generous PTO and company-observed holidays, 401(k) with employer match, professional development opportunities, and a people-first culture backed by Pine Services Group

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

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