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Csv Validation Engineer Jobs in Puerto Rico (NOW HIRING)

Validation & Engineering Group, Inc

PR

$57K - $58K/yr

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Associate CSV - Periodic Review Scientist Position Summary The Associate CSV Periodic Review ...

Validation & Engineering Group, Inc

PR

$59K - $60K/yr

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Associate CSV - Periodic Review Scientist Position Summary The Associate CSV Periodic Review ...

FITS LLC

Manufacturing Engineer I - 158

Villalba, PR · On-site

$70K - $91K/yr

For engineering services in the Manufacturing area. WHAT MAKES YOU A FIT: The Technical Part ... CSV Equipment Validation. * Cross-functional team collaboration The Personality Part: * Our Next ...

Mirus Consulting Group

CSV Specialist

Gurabo, PR

Its services include the assessment and validation of automation equipment, network infrastructures ... Bachelor's Degree in engineering, Computer Science, or a related scientific discipline. * Minimum ...

Mirus Consulting Group

CSV Specialist

Gurabo, PR · On-site

Its services include the assessment and validation of automation equipment, network infrastructures ... Bachelor's Degree in engineering, Computer Science, or a related scientific discipline. * Minimum ...

Mirus Consulting Group

CSV Specialist

Gurabo, PR

Its services include the assessment and validation of automation equipment, network infrastructures ... Bachelor's Degree in engineering, Computer Science, or a related scientific discipline. * Minimum ...

Weil Group, Inc.

Manufacturing Engineer II

Villalba, PR · On-site

$70K - $91K/yr

Highly desirable previous experience executing CSV validation of Equipment Controller in a facility ... Must collaborate with engineering process owners in development and execution of protocols. Must ...

Weil Group, Inc

Manufacturing Engineer II

Villalba, PR

$70K - $91K/yr

Highly desirable previous experience executing CSV validation of Equipment Controller in a facility ... Must collaborate with engineering process owners in development and execution of protocols. Must ...

Weil Group, Inc

Manufacturing Engineer II

Villalba, PR

$70K - $91K/yr

Highly desirable previous experience executing CSV validation of Equipment Controller in a facility ... Must collaborate with engineering process owners in development and execution of protocols. Must ...

Moriah Engineering

PR · On-site

$90K - $118K/yr

CSV Leadto oversee the validation of major capital automation projects. The ideal candidate will have extensive expertise in validation and compliance, computer system validation (CSV), and ...

Moriah Engineering

CSV Lead

Carolina, PR

$90K - $118K/yr

CSV Leadto oversee the validation of major capital automation projects. The ideal candidate will have extensive expertise in validation and compliance, computer system validation (CSV), and ...

Weil Group, Inc

CSV Specialist

Manati, PR · On-site

Perform Computerized System Validation (CSV) activities following site CSV Standard Procedure ... Bachelor's Degree in Engineering or Computer Science combined with three (3) years of CSV and ...

Moriah Engineering

CSV Project Manager

Jayuya, PR

Qualifications Bachelor's Degree Engineering, science or related field. Ability to plan, manage and ... Strong understanding of automation systems, PLCs, CSV, and related validation frameworks. Proven ...

Moriah Engineering

PR · On-site

Qualifications Bachelors Degree Engineering, science or related field. Ability to plan, manage and ... Strong understanding of automation systems, PLCs, CSV, and related validation frameworks. Proven ...

JC Automation Corp

PR · On-site

$25 - $35/hr

... and Engineering standards. * Validation Support: Assist in the execution of validation protocols, testing activities, CSV documentation authoring, and resolution of findings related to automation ...

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Csv Validation Engineer information

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.

What are popular job titles related to Csv Validation Engineer jobs in Puerto Rico? For Csv Validation Engineer jobs in Puerto Rico, the most frequently searched job titles are:
What job categories do people searching Csv Validation Engineer jobs in Puerto Rico look for? The top searched job categories for Csv Validation Engineer jobs in Puerto Rico are:
What cities in Puerto Rico are hiring for Csv Validation Engineer jobs? Cities in Puerto Rico with the most Csv Validation Engineer job openings:
Csv Validation Engineer jobs near you

Associate CSV - Periodic Review Scientist

Validation & Engineering Group, Inc

PR

$57K - $58K/yr

Full-time

Posted 19 days ago

Job description

Validation & 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:

  • Associate CSV – Periodic Review Scientist

Position Summary

The Associate CSV Periodic Review Scientist supports the execution of periodic reviews for GxP computer systems to ensure compliance with regulatory requirements and maintenance of the validated state. This entry-level role focuses on learning and applying validation principles, supporting risk-based assessments, and developing technical and compliance expertise in a GMP-regulated environment.

Key Responsibilities

  • Assist in the execution of Periodic Reviews (PR) for GxP computer systems under supervision.
  • Support the evaluation of:
    • Change controls, deviations, and CAPAs
    • System maintenance and calibration status
    • User access reviews and audit trails
    • Backup and restore processes
  • Help compile and organize documentation for PR reports.
  • Apply basic risk-based thinking to assess system status and identify potential issues.
  • Ensure documentation meets GDP (Good Documentation Practices) requirements.
  • Collaborate with cross-functional teams such as QA, IT, Engineering, and Operations.
  • Support audit and inspection readiness activities.
  • Follow procedures aligned with 21 CFR Part 11, EU Annex 11, and Data Integrity requirements.
  • Participate in training programs to build knowledge in CSV/CSA and GxP compliance.

Qualifications

  • Bachelor’s degree in:
    • Engineering (any discipline)
    • Computer Science / Information Systems
    • Life Sciences (Biology, Chemistry, Microbiology)
  • 0–2 years of experience in:
    • GMP environment, validation, IT, or quality (internships or co-ops acceptable)
  • Exposure to computer systems or regulated environments is a plus

Technical Skills

  • Basic understanding (or willingness to learn):
    • GxP regulations
    • Data Integrity (ALCOA+)
    • CSV/CSA concepts
  • Familiarity with:
    • Microsoft Office (Excel, Word, PowerPoint)
  • Exposure to GxP systems (SAP, LIMS, etc.) is a plus but not required

Preferred Qualifications

  • Internship experience in pharmaceutical, biotech, or regulated industries
  • Basic knowledge of validation lifecycle or system documentation
  • Exposure to audit or compliance activities

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.