Find a jobRecruiters

Computer System Validation (CSV) Specialist

Exclusive opportunity

Onsite

Computer System Validation (CSV) Specialist

ECHO Consulting Group Inc

Computer System Validation (CSV) Specialist

Skills

Testing & QASAP ERPCompliance

10 days ago

Share this opportunity

Share this opportunity to other talents of your network:
✓ Offer them a visibility boost with clients.
✓ Help your contacts find their next job.

Important information


Contract type:

Freelance / Contract

Location:

Manatí, 00674, Puerto Rico

Work mode:

Onsite

Published on:

16 October 2026

What they need


ECHO Consulting Group is a leader in providing solutions for the pharmaceutical, biotechnology, medical devices, and food industries. ECHO Consulting Group delivers high-quality solutions in CQV, quality management, regulatory compliance, manufacturing support, and project management. We are committed to offering exciting career opportunities in a workplace that values trust, respect, teamwork, creative talent, enthusiasm, and diligence. We are looking for talented professionals who are passionate about quality, collaboration, and delivering results. We believe great talent deserves great rewards. That’s why we offer a competitive compensation package and professional development.

Summary The CSV Specialist is responsible for planning, executing, and documenting computer system validation activities for GxP-regulated computerized systems within a pharmaceutical manufacturing environment. This role ensures that systems used in manufacturing, laboratory, and quality operations comply with FDA 21 CFR Part 11, GAMP 5, and applicable global regulatory requirements throughout the system lifecycle.

Responsibilities

  • Develop, review, and execute validation deliverables including Validation Plans, User Requirements Specifications (URS), Functional/Design Specifications, Risk Assessments, IQ/OQ/PQ protocols, and Validation Summary Reports.
  • Apply a risk-based approach (GAMP 5) to determine the appropriate level of validation rigor for each computerized system.
  • Validate GxP systems such as LIMS, MES, ERP, EDMS, building automation systems (BAS), historians, and other manufacturing/quality-related software and equipment interfaces.
  • Ensure compliance with 21 CFR Part 11, Annex 11, and data integrity principles (ALCOA+) across validated systems.
  • Author and execute test scripts, document deviations, and support root cause investigations and CAPAs related to system discrepancies.
  • Maintain the validated state of systems through periodic reviews, change control assessments, and revalidation activities.
  • Collaborate with IT, Quality, Engineering, and end users to support system implementations, upgrades, migrations, and decommissioning.
  • Support internal and external audits/regulatory inspections by providing validation documentation and responding to inspector questions.
  • Maintain accurate and audit-ready documentation in accordance with Good Documentation Practices (GDP).
  • Contribute to and help maintain site validation master plans (VMP) and SOPs related to computer system validation.

Education Bachelor's degree in Computer Science, Engineering, Life Sciences, Information Technology, or a related field required.

Location : Manatí, PR

Preferred Qualifications

  • 5+ years of experience in Computer System Validation within a pharmaceutical, biotech, or medical device environment.
  • Experience validating systems such as LIMS, MES, SCADA, ERP (e.g., SAP), EDMS, or Building Management Systems (BMS).
  • Familiarity with Agile/DevOps validation approaches and Computer Software Assurance (CSA) is a plus.
  • Experience supporting FDA, EMA, or other regulatory agency inspections.
  • ASQ CQE/CSSBB or similar quality certification is a plus.

Skills

  • Strong working knowledge of GAMP 5, 21 CFR Part 11, Annex 11, and data integrity requirements.
  • Proficiency in authoring and executing validation protocols (IQ/OQ/PQ) and technical documentation.
  • Solid understanding of SDLC (Software Development Life Cycle) and risk-based validation methodologies.
  • Strong analytical and problem-solving skills for troubleshooting and deviation investigations.
  • Excellent written and verbal communication skills, with the ability to interface with cross-functional teams (IT, QA, Engineering, Manufacturing).
  • Detail-oriented with strong organizational and time-management skills.
  • Proficiency with Microsoft Office and electronic quality management systems (eQMS).

Equal Employment Opportunity ECHO Consulting Group, Inc. is committed to providing equal employment opportunity without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status, or membership in any other class protected by federal, state, or local law.

We assure you that your opportunity for employment with ECHO Consulting Group, Inc. depends solely on your qualifications.

Other offers great for you!

These companies are also looking for great profiles

Vorstone

Finance System Specialist

520

Freelance

Lille, France

Hybrid

Skills

AccountingSpécialiste Systèmes et Processus FinanceAnalyse de fluxAccompagnement Projets et Support OpérationnelRéférentiel Fiscal et Reporting

5 days ago

Quick apply

BEATRICE ROY RECRUTEMENT & CONSEILS

Resources Manager System h/f

70 000 € - 80 000 €

Permanent contract

Moirans, France

Hybrid

Skills

Embedded SystemsElectronicsSignal processingVision systems

1 day ago

Quick apply

Futurwork

Patching & Automation Specialist

Permanent contract

Belgium

Hybrid

Skills

PythonAnsibleServiceNowPatch management automationPowerShellLinux and Windows Server

20 hours ago

Quick apply

The best place to find your next move

© 2026. All Rights Reserved.

Talents

Find a job

Create a profile

Solutions and tools