Computer System Validation Engineer Specialist

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profile Job Location:

Cork - Ireland

profile Monthly Salary: Not Disclosed
Posted on: 16 hours ago
Vacancies: 1 Vacancy

Job Summary

Advanced Manufacturing Tech Solutions (AMTSOL) -

A Leader in Life science Manufacturing Technology solutions we are looking for top talent to be part of the dynamic team and drive the growth of the business.

Job Title: Computer System Validation (CSV) Engineer / Specialist

Role Overview

We are looking for a Mid-Level CSV Engineer to support validation activities for GMP-regulated computerized systems across manufacturing packaging and laboratory environments. The role focuses on hands-on execution of CSV lifecycle deliverables working closely with Quality Engineering IT and project teams to ensure compliance and timely delivery.

Key Responsibilities

  • Execute CSV lifecycle activities for GMP computerized systems including MES DCS SCADA and automated equipment
  • Prepare review and support approval of CSV documentation (Validation Plans URS Risk Assessments IQ/OQ/PQ Reports)
  • Support risk-based validation approaches for new and existing systems
  • Ensure CSV activities comply with cGMP GAMP 5 Annex 11 and 21 CFR Part 11
  • Support project teams to align validation activities with project timelines
  • Participate in validation risk assessments to define appropriate testing scope
  • Review system specifications design documents installation records and qualification documentation
  • Support CSV activities across manufacturing packaging and laboratory systems
  • Generate track and support closure of validation deviations and discrepancies
  • Support investigations and assess data integrity risks during validation and routine operations
  • Perform periodic reviews of computerized systems and assist in identifying compliance gaps
  • Support the development and maintenance of CSV / Qualification SOPs
  • Assist in regulatory inspections and internal audits
  • Collaborate with local and global CSV teams to ensure consistent execution
  • Escalate potential quality or compliance issues to senior CSV or Quality leads
  • Follow EHS and site safety procedures during commissioning and validation activities

Qualifications & Experience

  • Bachelors degree in Engineering Life Sciences Computer Science or related discipline
  • 47 years of experience in Computer System Validation within a regulated pharma / biopharma environment
  • Solid understanding of CSV regulations and quality expectations
  • Hands-on experience validating GAMP Category 3 4 and 5 systems
  • Experience executing validation protocols and managing validation documentation
  • Working knowledge of Annex 11 21 CFR Part 11 and GAMP guidelines
  • Experience supporting investigations root cause analysis and CAPAs
  • Strong documentation and cross-functional collaboration skills
Advanced Manufacturing Tech Solutions (AMTSOL) - A Leader in Life science Manufacturing Technology solutions we are looking for top talent to be part of the dynamic team and drive the growth of the business. Job Title: Computer System Validation (CSV) Engineer / Specialist Role Overview We are l...
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Key Skills

  • Python
  • SOC
  • Debugging
  • C/C++
  • FDA Regulations
  • Minitab
  • Technical Writing
  • GAMP
  • OS Kernels
  • Perl
  • cGMP
  • Manufacturing