Computer System Validation (CSV) Specialist Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology ...
Computer System Validation (CSV) Specialist Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology ...
0065V6421 CSV Engineer (Laboratory)/Validation Engineer 2 Consultant Please contact Amanda Mazza, [email protected] Job Overview: We are seeking an experienced CSV Engineer to support the ...
0065V6421 CSV Engineer (Laboratory)/Validation Engineer 2 Consultant Please contact Amanda Mazza, [email protected] Job Overview: We are seeking an experienced CSV Engineer to support the ...
0065V6421 CSV Engineer (Laboratory)/Validation Engineer 2 Consultant Please contact Amanda Mazza, amanda@tworivercp.com Job Overview: We are seeking an experienced CSV Engineer to support the ...
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0065V6421 CSV Engineer (Laboratory)/Validation Engineer 2 Consultant Please contact Amanda Mazza, amanda@tworivercp.com Job Overview: We are seeking an experienced CSV Engineer to support the ...
Job Title - CSV Consultant Location - Raritan, NJ(Hybrid) Job Details: Role Overview: * Must be ... Infrastrucure Qualifications and Business Systems Validations * 10+ years of relevant experience ...
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Job Title - CSV Consultant Location - Raritan, NJ(Hybrid) Job Details: Role Overview: * Must be ... Infrastrucure Qualifications and Business Systems Validations * 10+ years of relevant experience ...
0065V6421 CSV Engineer (Laboratory)/Validation Engineer 2 Consultant Please contact Amanda Mazza: amanda@tworivercp.com Job Overview We are seeking an experienced CSV Engineer to support the ...
0065V6421 CSV Engineer (Laboratory)/Validation Engineer 2 Consultant Please contact Amanda Mazza: amanda@tworivercp.com Job Overview We are seeking an experienced CSV Engineer to support the ...
CSV Consultant
Raritan, NJ ยท On-site
We are seeking an experienced CSV Consultant with expertise in Computer System Validation (CSV) , SAP ERP , and Generative AI/Agentic AI in a GxP-regulated environment . The ideal candidate will have ...
CSV Consultant
Raritan, NJ ยท On-site
We are seeking an experienced CSV Consultant with expertise in Computer System Validation (CSV) , SAP ERP , and Generative AI/Agentic AI in a GxP-regulated environment . The ideal candidate will have ...
CSV, Analytical, and Enterprise Validation Specialist IV Experience Required: 5-10 years Education: Bachelor of Science in a science-related discipline or relevant field experience The CSV ...
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CSV, Analytical, and Enterprise Validation Specialist IV Experience Required: 5-10 years Education: Bachelor of Science in a science-related discipline or relevant field experience The CSV ...
CSV Consultant
Raritan, NJ ยท On-site
$45 - $50/hr
We are seeking an experienced CSV Consultant with expertise in Computer System Validation (CSV) , SAP ERP , and Generative AI/Agentic AI in a GxP-regulated environment . The ideal candidate will have ...
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CSV Consultant
Raritan, NJ ยท On-site
$45 - $50/hr
We are seeking an experienced CSV Consultant with expertise in Computer System Validation (CSV) , SAP ERP , and Generative AI/Agentic AI in a GxP-regulated environment . The ideal candidate will have ...
Manager, Computer Systems Validation (CSV)
Redwood City, CA ยท On-site
$160K - $189K/yr
The Manager, Computer Systems Validation (CSV) will be a core member of the Quality Systems Technology team and responsible for the implementation, management, ongoing support and review of Corcept ...
Manager, Computer Systems Validation (CSV)
Redwood City, CA ยท On-site
$160K - $189K/yr
The Manager, Computer Systems Validation (CSV) will be a core member of the Quality Systems Technology team and responsible for the implementation, management, ongoing support and review of Corcept ...
Digital Engineer - POMS MES Remote W2 Hiring.
Chicago, IL ยท On-site +1
Strong MES, EBR, workflows, GMP/GxP, CSV validation * Troubleshooting, documentation, compliance (FDA 21 CFR Part 11, GAMP 5) Optional Skills: * Largescale MES rollout, ERP/LIMS/SCADA integration
Digital Engineer - POMS MES Remote W2 Hiring.
Chicago, IL ยท On-site +1
Strong MES, EBR, workflows, GMP/GxP, CSV validation * Troubleshooting, documentation, compliance (FDA 21 CFR Part 11, GAMP 5) Optional Skills: * Largescale MES rollout, ERP/LIMS/SCADA integration
CSV Specialist
Gurabo, PR ยท On-site
Its services include the assessment and validation of automation equipment, network infrastructures and business processes, as well as the project management involved. Position Summary: The CSV ...
CSV Specialist
Gurabo, PR ยท On-site
Its services include the assessment and validation of automation equipment, network infrastructures and business processes, as well as the project management involved. Position Summary: The CSV ...
CSV Specialist
Gurabo, PR ยท On-site
Its services include the assessment and validation of automation equipment, network infrastructures and business processes, as well as the project management involved. Position Summary: The CSV ...
CSV Specialist
Gurabo, PR ยท On-site
Its services include the assessment and validation of automation equipment, network infrastructures and business processes, as well as the project management involved. Position Summary: The CSV ...
Company Description * Computer System Validation (CSV) of SAP (ERP) system to meet GxP compliance. * Validation is lean and risk based and is being built on previous validation deliverables.
Company Description * Computer System Validation (CSV) of SAP (ERP) system to meet GxP compliance. * Validation is lean and risk based and is being built on previous validation deliverables.
Computer System Validation Specialist Position Summary We are seeking a Computer System Validation (CSV) Specialist/Engineer to support validation activities for computerized systems in a regulated ...
Computer System Validation Specialist Position Summary We are seeking a Computer System Validation (CSV) Specialist/Engineer to support validation activities for computerized systems in a regulated ...
Computer System Validation Specialist Position Summary We are seeking a Computer System Validation (CSV) Specialist/Engineer to support validation activities for computerized systems in a regulated ...
Computer System Validation Specialist Position Summary We are seeking a Computer System Validation (CSV) Specialist/Engineer to support validation activities for computerized systems in a regulated ...
Digital Engineer - POMS MES Remote W2 Hiring.
Chicago, IL ยท On-site +1
Strong MES, EBR, workflows, GMP/GxP, CSV validation * Troubleshooting, documentation, compliance (FDA 21 CFR Part 11, GAMP 5) Optional Skills: * Large-scale MES rollout, ERP/LIMS/SCADA integration
Digital Engineer - POMS MES Remote W2 Hiring.
Chicago, IL ยท On-site +1
Strong MES, EBR, workflows, GMP/GxP, CSV validation * Troubleshooting, documentation, compliance (FDA 21 CFR Part 11, GAMP 5) Optional Skills: * Large-scale MES rollout, ERP/LIMS/SCADA integration
Senior CSV Engineer
Indianapolis, IN ยท On-site
$115K - $135K/yr
About Us Here at Performance Validation, Inc. (PV) we have been providing Commissioning ... Q and CSV documentation -- User Requirements, Functional and Design Specifications, Validation ...
Senior CSV Engineer
Indianapolis, IN ยท On-site
$115K - $135K/yr
About Us Here at Performance Validation, Inc. (PV) we have been providing Commissioning ... Q and CSV documentation -- User Requirements, Functional and Design Specifications, Validation ...
CSV Engineer
Redwood City, CA ยท On-site
Katalyst CRO is looking for an experienced and well-rounded CSV (Computer System Validation) Consultant to support multiple ongoing projects within a pharmaceutical environment. The ideal candidate ...
CSV Engineer
Redwood City, CA ยท On-site
Katalyst CRO is looking for an experienced and well-rounded CSV (Computer System Validation) Consultant to support multiple ongoing projects within a pharmaceutical environment. The ideal candidate ...
Sr. CSV / Lab Instrument Validation Specialist Type of role: Contract Duration: 12-36+ months Hourly pay rate: DOE (C2C, W2, or 1099 permissible) Location: South San Francisco Bay Area (Remote during ...
Sr. CSV / Lab Instrument Validation Specialist Type of role: Contract Duration: 12-36+ months Hourly pay rate: DOE (C2C, W2, or 1099 permissible) Location: South San Francisco Bay Area (Remote during ...
Validation Engineer
Greenville, NC ยท On-site
Lead full validation lifecycle activities ... FAT, SAT, CSV, equipment integration, and startup. * Drive process design for new equipment and ...
Validation Engineer
Greenville, NC ยท On-site
Lead full validation lifecycle activities ... FAT, SAT, CSV, equipment integration, and startup. * Drive process design for new equipment and ...
Csv Validation information
See salary details
$22.60 - $27.64
2% of jobs
$27.64 - $32.69
6% of jobs
$32.69 - $37.74
13% of jobs
$39.32 is the 25th percentile. Wages below this are outliers.
$37.74 - $42.79
13% of jobs
$42.79 - $47.84
11% of jobs
The median wage is $50.36 / hr.
$47.84 - $52.88
12% of jobs
$52.88 - $57.93
9% of jobs
$61.82 is the 75th percentile. Wages above this are outliers.
$57.93 - $62.98
13% of jobs
$62.98 - $68.03
13% of jobs
$68.03 - $73.08
6% of jobs
$73.08 - $78.13
3% of jobs
$22
$51
$78
How much do csv validation jobs pay per hour?
What is a csv validation?
A CSV Validation job involves verifying the accuracy, consistency, and integrity of data within CSV files. This role ensures that the data conforms to predefined formats, standards, and business rules. It often includes checking for missing values, incorrect data types, and formatting errors to prevent issues in data processing. Professionals in this role may use scripts, validation tools, or manual reviews to ensure data quality and compliance.
What are the typical daily responsibilities of a csv validation professional?
CSV (Computer System Validation) Validation professionals are responsible for planning, executing, and documenting validation activities for computerized systems used in regulated industries like pharmaceuticals and biotechnology. Their daily tasks include reviewing system requirements, developing validation protocols, conducting risk assessments, performing validation testing, and documenting results in accordance with regulatory standards. They regularly collaborate with IT, quality assurance, and business stakeholders to ensure systems are compliant and audit-ready. Staying organized and detail-oriented is crucial, as each step must be carefully documented and verified for compliance. This role is dynamic and requires balancing technical tasks with frequent cross-functional communication.
What are the key skills and qualifications needed to thrive in the csv validation position, and why are they important?
To excel in CSV Validation, a strong background in life sciences, engineering, or a related technical discipline is essential, along with knowledge of computer system validation regulations and best practices. Familiarity with FDA 21 CFR Part 11, GAMP guidelines, and validation software tools is highly valued, and certifications such as PMP or CISA can be beneficial. Attention to detail, analytical thinking, and effective communication skills help professionals manage documentation and collaborate with cross-functional teams. These abilities ensure that systems in regulated environments are compliant, reliable, and meet industry standards for quality and data integrity.
What cities are hiring for Csv Validation jobs?
Cities with the most Csv Validation job openings:
What are the most commonly searched types of Csv Validation jobs?
The most popular types of Csv Validation jobs are:
What states have the most Csv Validation jobs?
States with the most job openings for Csv Validation jobs include:
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Computer System Validation (CSV) Specialist
Wilson, NC โข On-site
Other
Posted 10 days ago
Job description
Current job opportunities are posted here as they become available.
Computer System Validation (CSV) SpecialistValidation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:
- Computer System Validation Specialist
Position Summary
We are seeking a Computer System Validation (CSV) Specialist/Engineer to support validation activities for computerized systems in a regulated manufacturing environment. The ideal candidate will have 3โ4 years of handsโon CSV experience and a solid understanding of GxP requirements, system lifecycle documentation, and data integrity principles.
Key Responsibilities
- Support the validation and lifecycle management of GxP computerized systems.
- Develop, review, and execute validation documentation, including:
- User Requirements Specifications (URS)
- Functional/Design Specifications
- Risk Assessments
- Validation Plans
- IQ/OQ/PQ protocols
- Test Scripts
- Traceability Matrices
- Validation Summary Reports
- Execute and document system testing and ensure appropriate resolution of discrepancies and deviations.
- Support system implementation, upgrades, enhancements, and periodic reviews.
- Perform computerized system risk assessments in accordance with applicable regulatory requirements and company procedures.
- Ensure compliance with 21 CFR Part 11, GxP, data integrity, and electronic records/electronic signature requirements.
- Collaborate with IT, Engineering, Quality, Manufacturing, Automation, and system owners throughout the system lifecycle.
- Support change controls, deviations, CAPAs, and system retirement activities as applicable.
- Assist with audit and inspection readiness activities related to computerized systems.
- Maintain accurate and complete validation documentation in accordance with approved procedures.
Qualifications
- Bachelorโs degree in Engineering, Computer Science, Information Technology, Life Sciences, or a related technical discipline.
- 3โ4 years of experience in Computer System Validation (CSV) within a regulated environment, preferably pharmaceutical, biotechnology, medical device, or life sciences manufacturing.
- Working knowledge of GAMP 5, 21 CFR Part 11, GxP, and data integrity principles.
- Experience developing and executing computerized system validation documentation and testing.
- Strong documentation, analytical, and problemโsolving skills.
- Ability to work crossโfunctionally with technical and quality teams.
- Strong written and verbal communication skills.
Preferred Qualifications
- Experience with Power BI for dashboards, reporting, data visualization, or analytics.
- Experience validating manufacturing, laboratory, quality, or enterprise systems.
- Experience supporting system upgrades, implementation projects, or digital transformation initiatives.
At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.