Validation Engineer – GMP Quality Oversight

About the role

PSC Biotech is seeking a Validation Engineer to join its Quality Assurance Validation team in Ireland. The role is a 12‑month fixed‑term contract with the possibility of extension, providing the opportunity to work on GMP‑regulated validation projects across manufacturing, equipment, computer, and laboratory systems.

Key responsibilities

• Act as the Subject Matter Expert (SME) and Quality Oversight representative for assigned validation disciplines.
• Maintain up‑to‑date knowledge of industry standards and regulatory requirements for validation techniques.
• Support the QA Validation group in ensuring regulatory compliance and best‑practice implementation.
• Assist with complex investigations, regulatory submissions, agency inspections, and specific regulatory queries.
• Develop validation strategies and ensure compliance throughout project lifecycles.
• Mentor junior QA Validation team members and provide cross‑functional SME support.
• Lead QA Validation representation in multi‑departmental meetings and project teams.
• Identify and drive improvements to validation systems and processes.

Required profile

• High level of initiative, energy, motivation and strong organisational skills.
• Eligibility to work full‑time in Ireland (EU, UK or Stamp 4 visa holders).
• Experience working in a GMP‑regulated environment, preferably within pharma/biotech.

Required skills

What we offer

• Exposure to top pharmaceutical client sites in a multicultural setting.
• Permanent‑style employment benefits and career development through in‑house training and mentorship.
• Potential for contract extension based on performance.