CSV Engineer

Project overview

CSV Engineer is required by CareerWise Recruitment for our Waterford based client .

Contract Length: 12 Months

Responsibilities

• Execute and support the full computer system validation lifecycle, including planning, testing, implementation, and periodic review activities.
• Develop, review, and maintain validation documentation such as Validation Plans, Risk Assessments, IQ/OQ/PQ protocols, Traceability Matrices, and Summary Reports.
• Collaborate with Quality, IT, Engineering, and Operations teams to ensure systems comply with GxP, FDA 21 CFR Part 11, Annex 11, and company quality standards.
• Lead validation activities for new system implementations, upgrades, and infrastructure changes across manufacturing, laboratory, and business systems.
• Investigate and assess deviations, incidents, and change controls to determine validation impact and ensure continued compliance.
• Support internal audits and regulatory inspections by providing validation documentation and subject matter expertise as required.

Requirements

Please contact James Farrar today for further information email: [contact removed]

CareerWise Recruitment (In Search of Excellence) Established in 1999, CareerWise Recruitment specialises in recruitment of management and technical professionals for the life sciences, ICT, engineering, food and agri sectors. We operate out of multiple locations in Ireland and have offices in Cork, Shannon, Galway, Mayo and Dublin. By applying for this position, you are consenting to allow CareerWise Recruitment to process and retain your data in accordance with our Privacy Policy, contained on our website for the purposes of providing career opportunities.

CareerWise Recruitment accepts that you do not wish your personal data, including your CV, to be forwarded to any client company without your prior consent and gives an absolute assurance that this wish will always be respected. Please feel free to contact us if you have any queries or wish to withdraw or amend your consent.

• Experience with Computer System Validation (CSV) for manufacturing, laboratory, utility, or quality systems.
• Validation of PLC, SCADA, HMI, and automated control systems.
• Experience with data integrity assessments and Annex 11 / 21 CFR Part 11 compliance.
• Experience supporting GMP inspections, audits, and CAPEX project delivery within regulated pharmaceutical environments. Required Experience & Qualifications
• Degree or equivalent qualification in Engineering, Computer Science, Life Sciences, or a related technical discipline.
• 3-5 years' experience within a pharmaceutical, biotechnology, medical device, or other GMP-regulated manufacturing environment.
• 2-3 years' experience in Computer System Validation (CSV), Validation, Automation, or a related compliance-focused role.
• Strong knowledge of GAMP 5, CSV lifecycle activities, cGMP requirements, and relevant regulatory expectations.
• Experience generating and executing validation documentation including DQ, IQ, OQ, PQ, and validation reports. Experience with change control, deviation management, and maintaining validated systems throughout their lifecycle

Project details

• Start: flexible
• Location: Waterford, IE