Computer Systems Validation - Consultant- Hybrid

Deloitte Ireland; Cork; Hybrid; EUR 41,000 - 50,000; Full time

Job summary

Deloitte Ireland is seeking a Computerised System Validation (CSV) specialist to support clients in the Life Sciences and Healthcare sectors from Cork or Limerick with a hybrid working model. You will lead validation activities to ensure regulatory compliance and data integrity, leveraging GAMP 5 and risk-based approaches.

Key responsibilities include advising on CSV best practices, managing change controls, and driving inspection readiness.

Qualifications

• Software/IT/Pharma/Science degree or related discipline.
• Experience in IT-related field; familiarity with JIRA, Trackwise, Veeva Vault.
• Understanding of SDLC with Agile or Waterfall.
• Experience validating computerised systems with AI integration.
• Experience in regulated industries and knowledge of GxP (GAMP, FDA/EMA).
• Proficiency with MS Office Tools.
• CAPA lifecycle and audit readiness experience.

Responsibilities

• Prepare, execute and review CSV validation deliverables in line with FDA/EMA/ICH regs.
• Advising clients in CSV best practice and regulatory compliance
• Complete validation activities to client requirements
• Support client in risk-based approach and identify process improvements
• Provide CSV guidance to project teams for documentation and test defects
• Monitor systems and processes to ensure SOP compliance and audit readiness
• Manage validation change control docs and support CAPA/quality metrics
• Apply risk-based validation to assess impact and ensure GAMP 5/data integrity
• Drive inspection readiness activities including gap assessments and mock audits

Skills

A flair for technology and computing

AI integration experience

SDLC & Agile/Waterfall understanding

MS Office proficiency

Regulated industries experience

Education

Software, IT, Pharma, Science degree or related discipline

Tools

JIRA

Trackwise

Veeva Vault

Job description

Why you'll enjoy this new opportunity

Deloitte is the world's number one professional services firm and making an impact is more than what we do. It is why we are here. We bring challenge, curiosity and edge to every project, driving positive progress for our clients, our people, our communities and the planet. This purpose inspires us to work to the highest standards and to tackle the challenges that matter. Number one never stops challenging.

Audit and Assurance is one of Deloitte Ireland's largest service lines and a core engine of our business. As the world's number one professional services firm, we bring challenge, curiosity and edge to the financial reporting ecosystem. We deliver insight, confidence and value for leading local and international clients.

Our teams combine advanced technology with deep professional expertise to evolve our audit and assurance processes. You will work with talented colleagues across our global network to make an impact that matters every day. Number one never stops challenging and neither do we.

We offer a competitive starting salary of €45,000.00 for this role, with salary adjustments reflecting your experience level and expertise.

Why you'll enjoy this new opportunity

Deloitte is the world's number one professional services firm and making an impact is more than what we do. It is why we are here. We bring challenge, curiosity and edge to every project, driving positive progress for our clients, our people, our communities and the planet. This purpose inspires us to work to the highest standards and to tackle the challenges that matter. Number one never stops challenging.

Audit and Assurance is one of Deloitte Ireland's largest service lines and a core engine of our business. As the world's number one professional services firm, we bring challenge, curiosity and edge to the Life Sciences sector. We deliver insight, confidence and value for local and international clients. You will work with talented colleagues across our global network to make an impact that matters every day. Number one never stops challenging and neither do we.

Key skills and prior experience that align well with this position

• Software, IT, Pharma, Science degree or related discipline
• Proven experience in IT related field; experience in systems such as JIRA, Trackwise, Veeva Vault
• A flair for technology and computing
• Experience of validating computerised systems with AI integration is preferable but not essential
• Experience in working in regulated industries preferable; solid understanding of EudraLex Volume 4, including Annex 11, FDA 21 CFR 11 and Good Automation practices (GAMP)
• Understanding of SDLC and methodologies such as Agile and Waterfall
• Basic understanding of quality management systems and data integrity principles
• Experience managing CAPA lifecycle activities, supporting inspection readiness for Food and Drug Administration (FDA) or European Medicines Agency (EMA) audits
• Experience applying 21 CFR Part 11, European Union Annex 11, GAMP 5, and data integrity requirements, including ALCOA+ principles
• Proficiency with MS Office Tools

What type of work will I be doing?

• Prepare and execute, and review validation deliverables for computerised systems in compliance with FDA, EMA, ICH, and other relevant regulations
• Advising clients in CSV best practice and regulatory compliance
• Completing validation activities to client requirements
• Supporting client in risk based approach and identify process improvement opportunities
• Providing CSV guidance and support to project teams in the resolution of validation documentation corrections and/or test defects
• Proactively monitor systems and processes to ensure compliance with standard operating procedures, audit requirements and industry best practices
• Manage validation change control documentation and support CAPA and quality metrics programmes
• Apply risk-based validation principles to assess system impact, classify validation requirements, and support compliance with GAMP 5 and data integrity expectations
• Drive inspection readiness activities, including gap assessments, mock audits, validation package reviews, and support for regulatory inspections and responses

Who is the Hiring Manager?

The hiring manager is a Senior Manager in the Audit and Assurance team in Deloitte and specialises in Computerized System Validation (CSV). They supports the delivery of validation solutions for clients in the Life Sciences and Healthcare industries and has extensive experience in CSV with expertise in Agile Methodologies and in the core cGMP requirements related to CSV, required to deliver CSV in the highly regulated life sciences industry. They are experienced in advising clients in CSV best practice and leading CSV project engagements with the client including delivering policies, procedures and conducting validation activities to client requirements.

Where is this role based?

This role is based in our Cork or Limerick offices with a flexible hybrid working model that supports a blend of of