Find Mes validation Jobs in Midleton, C

MES VALIDATION ENGINEER
Réalta Technologies (RT) —Cork, County Cork
- Full-time
- Computer Science
- Engineering
- No degree
6d
Senior MES Engineer Syncade
Cognizant —Cork, County Cork
- Full-time
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- Communication skills
MES Engineer Tulip
Cognizant —Cork, County Cork
- Full-time
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Senior Specialist - Industry 4.0 & Manufacturing Data
Deep DSG —Cork, County Cork
- Full-time
- Hybrid work
- Computer Science
- Master's degree
- SQL
- Annual leave
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Quick apply
IT Validation Specialist
Catalyx —Cork, County Cork
- Computer Science
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Senior MES Recipe Author
Cognizant —Cork, County Cork
- Full-time
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LEAD AUTOMATION ENGINEER
Réalta Technologies (RT) —Cork, County Cork
- Full-time
- System design
- Leadership
MES Engineer (POMSnet)
NeoDyne —Cork, County Cork
- Overtime
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Quick apply
Automation Engineer DeltaV
Cognizant —Cork, County Cork
- Full-time
- Hybrid work
- No degree
6d
Global Operational Technology Engineer
PepsiCo —Cork, County Cork
- Computer Science
- SQL
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MES VALIDATION ENGINEER

Réalta Technologies (RT)
Cork, County Cork

Apply Now

Job details

Full-time
6 days ago

Qualifications

Computer Science
Engineering
Communication skills

Full job description

FULL TIME

Cork, Ireland

Réalta Technologies is seeking an MES Validation Engineer to join a Digital Batch Record (DBR) implementation project at a leading pharmaceutical manufacturing facility in Cork.

Working alongside the Lead MES Validation Engineer, you will play a key role in supporting the validation lifecycle as the project progresses through the design approval and testing phases. This is an exciting opportunity to contribute to the successful deployment of Emerson Syncade MES within a GMP-regulated environment, ensuring the solution is delivered to the highest quality and compliance standards.

Job Responsibilities

Support the validation of Emerson Syncade MES as part of a Digital Batch Record (DBR) implementation project.
Review and approve design documentation, including Functional and Design Specifications, ensuring compliance with GMP and project requirements.
Author, review and execute validation documentation including Validation Plans, IQ, OQ and test protocols.
Perform system testing, document test results, investigate defects and support issue resolution throughout the validation lifecycle.
Maintain traceability between user requirements, functional specifications and validation deliverables.
Collaborate closely with MES, Automation, Quality, Manufacturing and Project teams to ensure successful project execution.
Ensure all validation activities are performed in accordance with GAMP5, CSV principles, site procedures and regulatory requirements.

Job Requirements

Degree in Engineering, Computer Science, Pharmaceutical Science or a related technical discipline.
3+ years' experience in MES Validation within a pharmaceutical or biotechnology GMP environment.
Hands-on experience with Emerson Syncade MES, ideally supporting Digital Batch Record (DBR) implementations.
Strong understanding of Computer System Validation (CSV), GAMP5, 21 CFR Part 11 and Annex 11 requirements.
Experience authoring and executing validation documentation including Validation Plans, IQ/OQ protocols, test scripts and traceability matrices.
Previous experience supporting design reviews, system testing and validation activities on pharmaceutical manufacturing projects.
Strong communication, documentation and stakeholder management skills, with the ability to work effectively in a hybrid, cross-functional project environment.

Apply Now

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mes validation jobs in midleton, c

MES VALIDATION ENGINEER

Senior MES Engineer Syncade

MES Engineer Tulip

Senior Specialist - Industry 4.0 & Manufacturing Data

IT Validation Specialist

Senior MES Recipe Author

LEAD AUTOMATION ENGINEER

MES Engineer (POMSnet)

Automation Engineer DeltaV

Global Operational Technology Engineer

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