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How much do part time computer system validation csv jobs pay per hour?

As of Jul 29, 2026, the average hourly pay for part time computer system validation csv in the United States is $51.80, according to ZipRecruiter salary data. Most workers in this role earn between $38.94 and $64.42 per hour, depending on experience, location, and employer.

What is the difference between Part Time Computer System Validation Csv vs Part Time Quality Assurance Specialist?

AspectPart Time Computer System Validation CsvPart Time Quality Assurance Specialist
CertificationsGxP, 21 CFR Part 11, CSV-specific trainingGxP, ISO, QA certifications
Work EnvironmentPharmaceutical, biotech, or healthcare industries focusing on computer systemsManufacturing, healthcare, or biotech industries focusing on product quality
Primary FocusValidating computer systems, ensuring compliance with regulationsMonitoring quality processes, audits, and compliance
Common UsageRegulatory submissions, validation documentationQuality audits, process improvements

While both roles involve compliance and industry standards, Part Time Computer System Validation Csv specifically focuses on validating computer systems to meet regulatory requirements, whereas Part Time Quality Assurance Specialist oversees overall quality processes and compliance. The CSV role is more technical and system-specific, while QA specialists handle broader quality assurance tasks across various processes.

How does a part-time Computer System Validation (CSV) specialist typically collaborate with cross-functional teams in regulated industries?

As a part-time CSV specialist, you will often work closely with quality assurance, IT, and operations teams to ensure that computer systems meet regulatory and compliance standards. Collaboration usually involves participating in validation planning sessions, reviewing documentation, and providing input during system implementation or upgrades. Even in a part-time capacity, effective communication and flexibility are crucial, as you may need to coordinate your schedule with project milestones and key team meetings. This collaborative environment provides valuable exposure to different departments and helps you build a versatile skill set.

What is a Part Time Computer System Validation (CSV) specialist?

A Part Time Computer System Validation (CSV) specialist is a professional who works on a part-time basis to ensure that computer systems used in regulated industries, such as pharmaceuticals or medical devices, meet compliance standards. Their responsibilities include planning, executing, and documenting validation activities to confirm that systems function as intended and adhere to regulatory requirements. These specialists often work with quality assurance, IT, and regulatory teams to maintain data integrity and support audits. Their part-time status allows organizations to access specialized expertise while managing costs.

What are the key skills and qualifications needed to thrive as a Part Time Computer System Validation (CSV) Specialist, and why are they important?

To excel as a Part Time Computer System Validation (CSV) Specialist, you need a solid background in computer science, life sciences, or engineering, along with knowledge of regulatory requirements such as FDA 21 CFR Part 11 and GxP guidelines. Familiarity with validation lifecycle documentation, risk management tools, and systems like SAP or LIMS, as well as certifications like PMP or Six Sigma, is highly valuable. Strong attention to detail, analytical thinking, and effective communication skills set outstanding CSV specialists apart. These competencies ensure validated systems meet compliance standards, maintain data integrity, and support safe, efficient business operations.
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Part Time Computer System Validation Csv jobs near you
Infographic showing various Part Time Computer System Validation Csv job openings in the United States as of July 2026, with employment types broken down into 100% Part Time. Highlights an 95% In-person, and 5% Remote job distribution, with an average salary of $107,747 per year, or $51.8 per hour.

CSV Engineer (Raleigh)

ALLIANCE BIOTECH SOLUTIONS LLC

Raleigh, NC • On-site

Part-time

Medical, Dental, Vision, Retirement, PTO

Posted 5 days ago

Job description

Description:


The Senior Computer System Validation (CSV) Engineer is responsible for leading the validation of complex computerized systems, custom-developed applications, enterprise databases, data platforms, and business intelligence solutions used within regulated GxP environments. This role partners with IT, Software Development, Data Engineering, Manufacturing, Quality, and business stakeholders to ensure that custom software applications, databases, reporting platforms, and system integrations are designed, validated, and maintained in compliance with regulatory requirements and industry best practices.

This position requires an experienced validation professional who is equally comfortable discussing validation strategy with Quality, reviewing software architecture with developers, validating SQL queries and database structures, and ensuring the integrity of data flowing between enterprise systems. The successful candidate will lead validation efforts across the full software development lifecycle, with particular emphasis on custom applications, relational databases, enterprise data warehouses/lakehouses, data pipelines, APIs, and business intelligence platforms that support manufacturing, laboratory, and business operations.

Requirements:


· Lead Computer System Validation (CSV) activities for custom-developed applications, enterprise databases, data platforms, dashboards, and other GxP computerized systems.

· Partner with software developers, data engineers, IT, Quality, and business stakeholders to define validation strategies and ensure compliance throughout the software development lifecycle.

· Author and execute validation deliverables including Validation Plans, URS, Risk Assessments, Traceability Matrices, IQ/OQ/PQ protocols, test scripts, and Validation Summary Reports.

· Validate custom applications, Power BI dashboards, enterprise databases, and cloud-based data platforms while performing SQL-based testing, data reconciliation, and verification activities.

· Validate system integrations, data pipelines, APIs, and interfaces between enterprise applications including LIMS, MES, ERP, PI Historian, and related GxP systems.

· Verify data integrity, security, audit trail, and electronic records controls to ensure compliance with GxP and regulatory requirements.

· Support audit readiness by maintaining compliant validation documentation and providing technical leadership on CSV, CSA, database validation, and data integrity best practices.


Experience & Skills


· Bachelor's degree in Engineering, Computer Science, Information Systems, Software Engineering, Life Sciences, or a related technical discipline.

· 7+ years of Computer System Validation (CSV) experience supporting custom software applications, enterprise databases, data platforms, and computerized systems within pharmaceutical, biotechnology, medical device, or other regulated industries.

· Demonstrated experience validating custom-developed applications, database-driven systems, enterprise integrations, and business intelligence platforms such as Power BI.

· Strong knowledge of relational databases, SQL, data architecture, data validation methodologies, and cloud-based data platforms such as Azure Data Lake, Databricks, Synapse, OneLake, SQL Server, Oracle, PostgreSQL, or similar technologies.

· Thorough understanding of GAMP 5, Computer Software Assurance (CSA), 21 CFR Part 11, EU Annex 11, ALCOA+ Data Integrity principles, and cGMP regulations.

· Experience leading validation efforts across the software development lifecycle, including requirements, risk assessments, testing, documentation, and audit readiness.

· Excellent analytical, troubleshooting, communication, and cross-functional collaboration skills.


Benefits & Compensation


• Industry competitive wage as a full-time employee

• Flexible Paid Time Off

• Bonus plans

• Medical, Dental and Vision Insurance with low employee cost

• Employer paid long term and short-term disability

• 401k plan with employer contributions


About Alliance Biotech Solutions


Alliance Biotech Solutions (ABS) is a premier consulting firm specializing in biopharmaceutical engineering and validation services. As industry leaders in Commissioning, Qualification, and Validation (CQV), we provide crucial services to the biotech and pharmaceutical sectors while maintaining our philosophy that employees are our #1 priority. Our success is built on the foundation of empowering our team members' growth and development, recognizing that our employees are the cornerstone of our clients' success.

Alliance Biotech Solutions is an Equal Employment Opportunity / Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, national origin, ancestry, citizenship status, military status, protected veteran status, religion, creed, physical or mental disability, medical condition, marital status, sex, sexual orientation, gender, gender identity or expression, age, genetic information, or any other basis protected by law, ordinance, or regulation.

Alliance Biotech Solutions does not accept unsolicited resumes through or from search firms or staffing agencies. All unsolicited resumes will be considered the property of Alliance Biotech Solutions, and Alliance Biotech Solutions will not be obligated to pay a placement fee.

All persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire.


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