Asks for

The ad says“Understanding of SDLC and methodologies such as Agile and Waterfall”
The ad says“Experience applying 21 CFR Part 11, European Union Annex 11, GAMP 5, and data integrity requirements, including ALCOA+ principles”
The ad says“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)”
The ad says“Experience managing CAPA lifecycle activities, supporting inspection readiness for Food and Drug Administration (FDA) or European Medicines Agency (EMA) audits”
The ad says“Basic understanding of quality management systems and data integrity principles”
The ad says“Experience managing CAPA lifecycle activities, supporting inspection readiness for Food and Drug Administration (FDA) or European Medicines Agency (EMA) audits”
The ad says“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)”
The ad says“Experience managing CAPA lifecycle activities, supporting inspection readiness for Food and Drug Administration (FDA) or European Medicines Agency (EMA) audits”
The ad says“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)”
The ad says“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)”
The ad says“Experience applying 21 CFR Part 11, European Union Annex 11, GAMP 5, and data integrity requirements, including ALCOA+ principles”
The ad says“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)”
The ad says“Proven experience in IT related field; experience in systems such as JIRA, Trackwise, Veeva Vault”
The ad says“Proficiency with MS Office Tools”
The ad says“Basic understanding of quality management systems and data integrity principles”
The ad says“Understanding of SDLC and methodologies such as Agile and Waterfall”
The ad says“Proven experience in IT related field; experience in systems such as JIRA, Trackwise, Veeva Vault”
The ad says“Proven experience in IT related field; experience in systems such as JIRA, Trackwise, Veeva Vault”
The ad says“Understanding of SDLC and methodologies such as Agile and Waterfall”

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.

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.
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Why you'll enjoy this new opportunity

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 office and remote working. Client site visits may be required depending on project needs. For more information, please visit our Deloitte Works webpage.

If you meet most of the criteria above, we encourage you to apply. Deloitte is an equal opportunities employer and will ensure that any reasonable accommodations are implemented throughout the recruitment and selection process.

What we offer

Your reward at Deloitte is competitive, purpose driven and designed to support your growth. It is more than salary. We invest in your personal and professional development, empower your work life balance and offer benefits that support you at every stage of life. These include health and wellbeing supports, pension and savings options, training and coaching and enhanced leave options.