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Csv Validation Engineer Jobs (NOW HIRING)

Syner-G

Validation Engineer

Waltham, MA · On-site +1

The Validation Engineer will play a key role in supporting operational readiness, tech transfer ... Handson validation experience in equipment, computerized systems (CSV), analytical methods, and ...

Syner-G

Validation Engineer

Waltham, MA · On-site

The Validation Engineer will play a key role in supporting operational readiness, tech transfer ... Demonstrated experience writing IQ, OQ, PQ, and CSV reports. Knowledge, Skills, and Abilities

Syner-G

Validation Engineer

Waltham, MA

The Validation Engineer will play a key role in supporting operational readiness, tech transfer ... Demonstrated experience writing IQ, OQ, PQ, and CSV reports. Knowledge, Skills, and Abilities

Katalyst CRO

CSV Engineer

Redwood City, CA · On-site

Katalyst CRO is looking for an experienced and well-rounded CSV (Computer System Validation ... CSV Engineer • Ensuring compliance with validation and regulatory standards Qualifications

TekWissen LLC

Senior Validation Engineer

Portsmouth, NH · On-site

$35 - $45/hr

Senior Validation Engineer Location: Portsmouth, NH - 03801 Duration: 7 Months Job Type: Temporary ... Hybrid Summary The CSV Engineer will act as an individual contributor responsible for ensuring ...

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How much do csv validation engineer jobs pay per hour?

As of Jul 22, 2026, the average hourly pay for csv validation engineer in the United States is $52.00, according to ZipRecruiter salary data. Most workers in this role earn between $39.42 and $63.22 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a CSV Validation Engineer, and why are they important?

To thrive as a CSV (Computer System Validation) Validation Engineer, you need expertise in validation methodologies, regulatory compliance (such as FDA 21 CFR Part 11), and a background in life sciences or engineering. Familiarity with validation tools, documentation systems, and quality management software is typically required, along with knowledge of industry standards like GAMP 5. Strong attention to detail, analytical thinking, and effective communication skills set outstanding candidates apart. These competencies ensure validated systems meet regulatory requirements, maintain data integrity, and support safe, compliant operations in regulated environments.

What are Csv Validation Engineers?

CSV Validation Engineers are professionals responsible for ensuring that computerized systems used in regulated industries, such as pharmaceuticals or biotechnology, comply with industry standards and regulations. CSV stands for Computer System Validation, which involves testing and documenting that systems function as intended and meet regulatory requirements for data integrity and security. These engineers typically create validation protocols, perform risk assessments, and support audits. Their work is crucial to ensure that electronic records and processes are reliable, traceable, and meet legal and industry guidelines.

What are some common challenges faced by a CSV Validation Engineer when working with cross-functional teams?

As a CSV Validation Engineer, one common challenge is ensuring clear communication and understanding between IT, QA, and business process teams regarding regulatory requirements and validation protocols. Misalignment on validation deliverables or timelines can occur, especially when teams have differing priorities or levels of familiarity with compliance frameworks. Proactively facilitating discussions, clarifying documentation, and providing training on Computer System Validation standards can help bridge gaps and keep projects on track.

What is the difference between Csv Validation Engineer vs Data Quality Analyst?

AspectCsv Validation EngineerData Quality Analyst
Required CredentialsBachelor's in Computer Science, Data Management, or related field; familiarity with data validation toolsBachelor's in Data Science, Statistics, or related; certifications like CDMP are common
Work EnvironmentData teams, software development, quality assuranceData analysis, reporting, data governance teams
Industry UsageTech, finance, healthcare, where data validation is criticalBusiness intelligence, analytics, data management sectors

The Csv Validation Engineer primarily focuses on validating and ensuring the accuracy of CSV data files through automated tools and scripts. In contrast, the Data Quality Analyst evaluates overall data quality, identifies issues, and implements data governance practices. Both roles require strong analytical skills and familiarity with data management, but their core responsibilities differ in scope and focus.

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Csv Validation Engineer jobs near you
Infographic showing various Csv Validation Engineer job openings in the United States as of July 2026, with employment types broken down into 2% As Needed, 84% Full Time, 3% Part Time, 1% Temporary, and 10% Contract. Highlights an 83% Physical, 3% Hybrid, and 14% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.
Sr. Manufacturing Engineer- Computer Systems Validation (CSV)

Sr. Manufacturing Engineer- Computer Systems Validation (CSV)

CIS International LLC

Juncos, PR

Full-time

Posted 5 days ago

Job description

Summary:
We are seeking an experienced Sr. Manufacturing Engineer – Computer Systems Validation (CSV) to support manufacturing operations in a regulated environment. This role is responsible for supporting IT system upgrades associated with manufacturing equipment, executing Computer System Validation (CSV) activities, and maintaining compliant validation documentation throughout the system lifecycle. The selected candidate will work closely with Manufacturing, Engineering, Quality, Validation, and Information Technology teams to ensure manufacturing systems remain compliant and operational.
Key Responsibilities:
  • Support IT system upgrades related to manufacturing equipment.
  • Execute Computer System Validation (CSV) activities in accordance with company procedures and regulatory requirements.
  • Develop, review, and maintain validation protocols, reports, and technical documentation.
  • Update manufacturing system documentation as required during system modifications and upgrades.
  • Coordinate and execute testing activities for manufacturing-related computerized systems.
  • Support integrations between manufacturing equipment and IT applications.
  • Assist with system implementation, troubleshooting, and validation activities.
  • Collaborate with cross-functional teams to ensure project milestones and validation deliverables are achieved.
  • Ensure compliance with applicable quality systems, validation standards, and regulatory requirements.
Minimum Qualifications:
  • Bachelor's degree in Engineering, Computer Engineering, Computer Science, Information Systems, or a related technical discipline.
  • Minimum of 5 years of experience in a regulated manufacturing environment (medical device, pharmaceutical, biotechnology, or similar).
  • Hands-on experience performing Computer System Validation (CSV).
  • Experience supporting manufacturing IT systems and integrations with manufacturing equipment.
  • Experience supporting computerized system upgrades and implementation projects.
  • Strong technical writing and documentation skills.
  • Excellent analytical, troubleshooting, and problem-solving abilities.
  • Ability to work independently and collaborate effectively with cross-functional teams.
  • Bilingual (English and Spanish) preferred.
Preferred Qualifications
  • Experience in FDA-regulated, cGMP, medical device, pharmaceutical, or biotechnology manufacturing.
  • Knowledge of GAMP 5, 21 CFR Part 11, Computerized System Lifecycle (CSLC), and Change Control processes.
  • Experience validating manufacturing software and computerized equipment systems.
Additional Requirements
  • Available to work overtime and weekends as required to support project schedules.
  • Strong organizational, communication, and interpersonal skills.
  • Ability to manage multiple priorities in a fast-paced manufacturing environment.

Work Methodology

  • 100% on site job
  • Full on-site job in Juncos, PR
  • Administrative shift
  • Duration: 6 months (1st contract) with a high possibility of extension based on performance and budget.
  • Type of industry: Medical devices
  • Expected hiring month: July 2026