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Part Time Computer System Validation Csv Jobs (NOW HIRING)

Eliquent Life Sciences, Inc

CSV Engineer

Mount Horeb, WI · On-site

$79K - $106.70K/yr

FDA and cGMP regulations and documentation practices Computer system validation methodologies ... Attractive salary and comprehensive benefits package for full-time and part-time employees ...

ClearanceJobs

Computer Operator 1 Jobs

Lemoore, CA · On-site

Part-Time Computer Operator I Valiant is looking for a Part-Time Computer Operator I to join our ... Possess the ability to obtain a US Passport and must have and maintain a valid driver's license.

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

As of May 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 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.

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 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.

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Part Time Computer System Validation Csv jobs near you

CSV Engineer

Eliquent Life Sciences, Inc

Mount Horeb, WI • On-site

$79K - $106.70K/yr

Full-time, Part-time

Medical, Dental, Vision, Life, Retirement, PTO

This job post has expired today. Applications are no longer accepted.

Job description

Job Description Job Description ELIQUENT Life Sciences is the leading global consulting firm providing solutions to life science companies researching, developing, and manufacturing innovative products to serve patients and respond to public health challenges around the world. ELIQUENT is committed to serving clients' needs with extensive expertise, unwavering integrity, and strategic insight in a manner that supports availability of safe, effective, and high-quality drugs, biologics, and medical devices. For more information, please visit our website at eliquent.com.

We are seeking a Computerized Systems Validation (CSV) Engineer experience to join our team. This role will focus on supporting laboratory and IT systems in regulated life sciences environments. The CSV Engineer will author validation deliverables—including protocols, reports, and SOPs—ensuring compliance with FDA, EMA, and global regulatory expectations.

Key Responsibilities: Develop and maintain Design Specifications (DS) for computerized and automated systems. Author and execute Installation Qualification (IQ) and Operational Qualification (OQ) protocols. Generate and review validation reports and Validation Summary Reports (VSRs).

Author and maintain Standard Operating Procedures (SOPs) for validated systems and equipment. Support implementation of CSV activities for IT and manufacturing automation systems in GMP environments. Apply risk-based validation approaches in alignment with industry standards and regulatory guidance.

Partner with Quality, Engineering, and IT teams to align validation deliverables with compliance and business needs. Contribute to inspection readiness by ensuring validation documentation meets regulatory expectations. Qualifications: Bachelor's degree in Engineering, Computer Science, Life Sciences, or related field.

2-10+ years of experience in computerized systems validation within pharmaceutical, biotechnology, or life sciences industries. Working knowledge of: FDA and cGMP regulations and documentation practices Computer system validation methodologies Strong technical writing skills with attention to detail. Direct experience with Evolve System preferred.

BENEFITS: What We Offer: Competitive Compensation: Attractive salary and comprehensive benefits package for full-time and part-time employees, including health, dental, vision, and life insurance, a 401(k) plan with employer match, a generous paid time off policy, and additional perks. Compensation is commensurate with professional experience. Career Development: Opportunities for professional growth and advancement within a supportive and innovative environment.

Work-Life Balance: Flexible work arrangements and a commitment to maintaining a healthy work-life balance. Eliquent Life Sciences is proud to be an Equal Opportunity Employer, committed to employee diversity.

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