Find Validation engineer automation Jobs in Dublin, D

CSV Engineer
Grifols Worldwide Op Ltd —Dublin, County Dublin
- Full-time
- Engineering
- Project management
- IT
13h
Instrumentation and Controls Engineer
IPS-Integrated Project Services —Dublin, County Dublin
- Full-time
- AutoCAD
- CAD
- Engineering
9h
Sr. Security Engineer - GRC EU/UK Regulation & Data Protection
SpaceXAI —Dublin, County Dublin
- Azure
- Computer Science
- Sales
Quick apply
7d
Transformation Governance Lead, Service Delivery, Trust and Safety
Google —Dublin, County Dublin
- €138,000–€141,000 a year
- Full-time
- Bachelor's degree
- No degree
- AI
11h
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
7h
Senior Azure Administrator
Version 1 —Dublin, County Dublin
- Up to €1 a month
- Full-time
- Azure
- Oracle
- Windows
- Employee assistance program
- Employee discount
Quick apply
Senior Electrical Commissioning Engineer
Winthrop Technologies —Dublin, County Dublin
- System design
- No degree
- HVAC
Quick apply
Cloud Platform Engineer
Grouper —Dublin, County Dublin
- Full-time
- Remote
- Azure
- Java
- AWS
Quick apply
Senior Automation Engineer
Embecta —Dún Laoghaire, County Dublin
- Full-time
- Engineering
- Bachelor's degree
- Manufacturing
Quick apply
Automation Engineering Leader
Embecta —Dún Laoghaire, County Dublin
- Full-time
- Engineering
- Bachelor's degree
- Manufacturing
Quick apply
Senior Process Engineer
Embecta —Dún Laoghaire, County Dublin
- Full-time
- Engineering
- Data analysis skills
- Bachelor's degree
Quick apply
Engineering Shift Technician
Embecta —Dún Laoghaire, County Dublin
- 12 hour shift
- Engineering
- Analysis skills
- Continuous improvement
Quick apply

Other jobs to consider

Find your next job by exploring related positions.

Quality Engineer - Fuze Services - Fixed Term Contract
Fuze Health —Northern Cross, County Dublin
Evaluate current products and processes to ensure ongoing compliance with applicable regulations and standards such as ISO 13485, 21 CFR Part 820, MDR 2017/745,…
€60,000–€68,000 a year
12d
Pre Sales Solution Engineer
Elwood Roberts —Dublin, County Dublin
Maintain current knowledge of industry trends, networking technologies, and partner roadmaps. Assist in product positioning and competitive analysis during the…
€60,000–€100,000 a month
Quick apply

I want to receive the latest job alerts for validation engineer automation in dublin, d

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

validation engineer automation jobs near dublin, d

Instrumentation Engineer jobs in Dublin, County Dublin

Senior Security Engineer jobs in Dublin, County Dublin

Senior Administrator jobs in Dublin, County Dublin

Platform Engineer jobs in Dublin, County Dublin

Engineer jobs in Dublin, County Dublin

Software Engineer jobs in Waterford, County Waterford

Process Engineer jobs in Waterford, County Waterford

Instrumentation Engineer jobs in Cork, County Cork

Engineer jobs in Dundalk, County Louth

Instrumentation Engineer jobs in Lucan, County Dublin

Junior Cloud Engineer jobs in Dublin, County Dublin

Semiconductor Engineer jobs in Dublin, County Dublin

Security Security jobs in Athlone, County Westmeath

Senior Hr jobs in Dublin, County Dublin

Finance Administrator jobs in Cork, County Cork

Senior Administrator jobs in Cork, County Cork

Part Time Administrator jobs in South Dublin, County Dublin

Senior Administrator jobs in Dublin 4, County Dublin

Senior Administrator jobs in Tallaght, County Dublin

Platform Engineer jobs in Limerick, County Limerick

CSV Engineer

Grifols Worldwide Op Ltd -
Dublin, County Dublin

Apply Now

Job details

Full-time
13 hours ago

Benefits

Private medical insurance

Qualifications

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

Full job description

table.MiTabla { max-width: 1020px;!important

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

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

Transformation Governance Lead, Service Delivery, Trust and Safety

Senior Business Systems Engineer

Senior Azure Administrator

Senior Electrical Commissioning Engineer

Cloud Platform Engineer

Senior Automation Engineer

Automation Engineering Leader

Senior Process Engineer

Engineering Shift Technician

Other jobs to consider

I want to receive the latest job alerts for validation engineer automation in dublin, d

Related Searches

Explore jobs in more locations

Jobseeker tools

Employer Tools

Browse

Stay Connected