Impactful Validation Engineer – Life Sciences (11-Month Contract)

QCS Staffing

Carlow

On-site

EUR 55,000 - 75,000

Full time

9 days ago

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Job summary

QCS Staffing is seeking a Validation Engineer for an initial 11‑month contract in Carlow, Ireland. The role focuses on validation of equipment and processes in a GMP environment, supporting QA and regulatory compliance, and driving validation strategies across projects.

You will work with cross‑functional teams to ensure robust qualification plans, root‑cause analyses, and timely resolution of deviations, while maintaining high documentation standards and contributing to audits and inspections.

Qualifications

  • Experience in equipment and process validation within GMP environments.
  • Knowledge of CTU qualification, thermal mapping, sterilisation (VHP, autoclave, SIP, dry heat) and sterile fill‑finish equipment.
  • Ability to analyse complex technical data, perform root cause analyses, and relate findings to equipment or process performance.
  • Strong communication and leadership skills, with experience writing high‑quality reports and coordinating across global teams.

Responsibilities

  • Design, review, approve, and execute qualification/validation documentation and studies to meet GMP/regulatory standards.
  • Troubleshoot and resolve issues during validation activities, performing root cause analysis.
  • Collaborate with Production, Maintenance, and Quality teams and act as validation representative for projects and global forums.
  • Support audits/inspections, complete risk assessments, and close out corrective actions.

Job description

QCS Staffing is seeking a Validation Engineer for an initial 11‑month contract in Carlow, Ireland. The role focuses on validation of equipment and processes in a GMP environment, supporting QA and regulatory compliance, and driving validation strategies across projects.

You will work with cross‑functional teams to ensure robust qualification plans, root‑cause analyses, and timely resolution of deviations, while maintaining high documentation standards and contributing to audits and inspections.

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