Find Validation engineer automation Jobs in Dublin, D

CSV Engineer
Grifols Worldwide Op Ltd —Dublin, County Dublin
- Full-time
- Engineering
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10h
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IPS-Integrated Project Services —Dublin, County Dublin
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Thermo Systems LLC —Dublin, County Dublin
- Full-time
- Software troubleshooting
- No degree
- In-person
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- Manufacturing
- Leadership
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- Azure
- Computer Science
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6d
Senior Business Systems Engineer
Foxit —Dublin, County Dublin
- €60,000–€72,000 a year
- Full-time
- Hybrid work
- Computer Science
- Analysis skills
- Bachelor's degree
Quick apply
5h
NPI Automation Engineer
oleson —Dublin, County Dublin
- Engineering
- In-person
CQV Engineer
CAI —Dublin, County Dublin
- Full-time
- Engineering
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Agentic Product Specialist – Manager
Pfizer —Dublin, County Dublin
- Full-time
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ASIC Digital Design, Principal Engineer
Synopsys —Dublin, County Dublin
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CQV Engineer
IPS-Integrated Project Services —DUBLIN 12, County Dublin
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Digital Operations Agentic Lead – Senior Manager
Pfizer —Dublin, County Dublin
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Senior Process Engineer
Jacobs —Dublin, County Dublin
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NNIT A/S —Dublin, County Dublin
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Innatera Nanosystems —Dublin, County Dublin
- Full-time
- Hybrid work
- Computer Science
- Master's degree
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DeltaV Engineer
Cognizant —Dublin, County Dublin
- Full-time
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Senior OSI PI Engineer
NNIT A/S —Dublin, County Dublin
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Senior Azure Administrator
Version 1 —Dublin, County Dublin
- Up to €1 a month
- Full-time
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Software Development Manager , AWS DMS
Amazon Development Centre Ireland Limited —Dublin, County Dublin
- Full-time
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Architect
TestReach —Dublin, County Dublin
- Azure
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CSV Engineer

Grifols Worldwide Op Ltd -
Dublin, County Dublin

Apply Now

Job details

Full-time
10 hours ago

Benefits

Private medical insurance

Qualifications

Engineering
Laboratory information management systems
Project management
IT
Communication skills
Information Technology

Full job description

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Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.

At Grifols, we believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunities that foster an inclusive environment.

Position Summary

We are looking for an experienced CSV Validation Engineer to join our Validation team. In this role, you will act as a subject matter expert (SME) for Computer System Validation (CSV) and validation activities across major capital projects.

You will play a key role in validating new software, automated equipment, manufacturing systems, and cloud-based platforms to ensure compliance with GMP, regulatory requirements, and data integrity standards.

This is an excellent opportunity for someone who enjoys working across Quality, Operations, IT, Engineering, and Maintenance teams while contributing to innovative projects in a highly regulated pharmaceutical environment.

What You'll Do

Write, review and execute Validation Protocols and Reports (for Equipment, software /automation, and enterprise software systems) ensuring compliance to all relevant global and local quality and validation procedures/standards
Review change controls and assess impact of changes that affect validated systems and define validation requirements
Represent Validation at both internal and external audits by regulatory agencies, including HPRA and FDA.
Generation and review of CSV project documentation (User Requirement Specifications, validation protocols, reports etc.) and Standard Operating Procedures.
Supporting validation activities including review of documentation hands-on execution of validation activities (FAT, SAT, IQ, OQ, PQ, UAT, etc) to ensure equipment /software meets current GMP requirements and industry standards.
Maintain the Site Validation Master Plan (VMP) and associated Project VMP’s, defining the validation approach associated with each piece of equipment, system, process and the requalification requirements including study requirements and frequency. Execute/Co-ordinate Re-Validation activities as required.
Completion of risk assessments, closure of corrective and preventive actions.
Develops alternative solutions to problems, handles Highly complexity problems independently. Demonstrates technical knowledge and ability to adapt to changing circumstances. Works with other departments Operations, Quality, IT and Maintenance) to lead qualification and validation efforts in support of site projects.

What You'll Bring

Degree in Science, Engineering, or a related discipline, with 3+ years' experience in CSV/CSA, Validation, or Quality within the biopharmaceutical industry.
Strong experience in Computer System Validation (CSV), Computer Software Assurance (CSA), and qualification of GxP systems and equipment.
Hands-on experience validating MES, EBR, LIMS, SaaS/cloud-based platforms, and automated systems such as SCADA, BMS, PCS, and DCS.
Proven experience executing the full equipment and system lifecycle, including FAT, SAT, DQ, IQ, OQ, PQ, QRM, and commissioning/qualification activities.
Solid knowledge of GxP, cGMP, FDA 21 CFR Part 11, EU Annex 1, data integrity requirements, and ISPE GAMP 5 guidelines.
Experience performing data integrity assessments, data mapping, and data governance activities in line with ALCOA principles.
Strong technical documentation skills, including the preparation and review of SOPs, validation plans, protocols, and reports.
Experience supporting and representing validation functions during internal, corporate, FDA, and HPRA audits.
Strong project management, analytical, problem-solving, communication, and stakeholder management skills, with the ability to work effectively across cross-functional teams.
Experience in an aseptic biopharmaceutical manufacturing environment and familiarity with biopharmaceutical IT infrastructure is highly desirable.

Our Benefits Include:
Highly competitive salary
Annual performance based bonus %
Shares options scheme
Group pension scheme - Contribution rates are (3%/ 5%/ 7%) and company will match
Private Medical Insurance for the employee
Ongoing opportunities for career development in a rapidly expanding work environment
Succession planning and internal promotions
Education allowance
Wellness activities - Social activities eg. Padel, Summer Events

We understand that self-doubt can hold talented individuals back from applying for opportunities. We encourage everyone who meets the qualifications to apply – we're excited to hear from you

#LI-FD1

Location: Grange Castle International Business Park, Grange, Co. Dublin, D22 K2R3

Learn more about Grifols

Apply Now

Refine Your Search

validation engineer automation jobs in dublin, d

CSV Engineer

Instrumentation and Controls Engineer

Commissioning Engineer

Technology Operational Readiness Lead – Drug Product Manufacturing

Sr. Security Engineer - GRC EU/UK Regulation & Data Protection

Senior Business Systems Engineer

NPI Automation Engineer

CQV Engineer

Agentic Product Specialist – Manager

ASIC Digital Design, Principal Engineer

CQV Engineer

Digital Operations Agentic Lead – Senior Manager

Senior Process Engineer

Senior Automation / OT Consultant

Senior SDK Hardware Simulator Engineer

DeltaV Engineer

Senior OSI PI Engineer

Senior Azure Administrator

Software Development Manager , AWS DMS

Architect

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