Computer System Validation (CSV) Specialist

ECHO Consulting Group
  • Manati, Puerto Rico
  • Autofill and Review
3 days ago

Job Description

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.

Numbers & Facts

LocationManati, Puerto Rico

Skills

  • Agile Programming Methodologiesunmatched
  • American Society for Quality (ASQ)unmatched
  • Automation Systemsunmatched
  • Biologyunmatched
  • Biotech and Pharmaceuticalunmatched
  • Certified Quality Engineer (CQE)unmatched
  • Change Controlunmatched
  • Code of Federal Regulationsunmatched
  • Communication Skillsunmatched
  • Computer Scienceunmatched
  • Computer Skillsunmatched
  • Computer Softwareunmatched
  • Computer Systemsunmatched
  • Consultingunmatched
  • Cross-Functionalunmatched
  • Customer Service Systemsunmatched
  • Data Qualityunmatched
  • DevOpsunmatched
  • Drug Manufacturingunmatched
  • ERP (Enterprise Resource Planning)unmatched
  • External Auditunmatched
  • FDA (Food and Drug Administration)unmatched
  • Food Deliveryunmatched
  • Food and Beverage Industryunmatched
  • GxPunmatched
  • Help Deskunmatched
  • Home Automationunmatched
  • Information Technology & Information Systemsunmatched
  • Internal Auditunmatched
  • Laboratory Information Management System (LIMS)unmatched
  • Laboratory Operationsunmatched
  • Maintain Complianceunmatched
  • Manufacturingunmatched
  • Manufacturing Requirementsunmatched
  • Manufacturing Systemsunmatched
  • Medical Equipmentunmatched
  • Microsoft Officeunmatched
  • Presentation/Verbal Skillsunmatched
  • Process Validationunmatched
  • Property Managementunmatched
  • Quality Assuranceunmatched
  • Quality Engineeringunmatched
  • Quality Managementunmatched
  • Regulationsunmatched
  • Regulatory Complianceunmatched
  • Regulatory Requirementsunmatched
  • Requirements Managementunmatched
  • Riskunmatched
  • Risk Analysisunmatched
  • Root Cause Analysisunmatched
  • SAPunmatched
  • Software Development Lifecycle (SDLC)unmatched
  • Standard Operating Procedures (SOP)unmatched
  • Supervisory Control and Data Acquisition (SCADA)unmatched
  • Support Documentationunmatched
  • System Lifecycleunmatched
  • System Validationunmatched
  • Systems Administration/Managementunmatched
  • Team Playerunmatched
  • Technical Writingunmatched
  • Technical/Engineering Designunmatched
  • Test Plan/Scheduleunmatched
  • Test Scriptsunmatched
  • Validation Documentationunmatched
  • Validation Planunmatched
  • Writing Skillsunmatched

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