Senior MES Recipe Author - Hybrid GMP Biotech Impact

Cognizant; Cork; Hybrid; EUR 65,000 - 90,000; Full time

Benefits offered by this job

Hybrid work model

Competitive salary and benefits

Job summary

Cognizant Ireland is seeking a Senior MES Recipe Author to implement System/MES recipe changes and manage day-to-day issues in the support of Electronic Batch Records, Weigh and Dispense, and Equipment Management modules on the Emerson Syncade MES solution at a large biotech facility in Cork.

You will operate in a collaborative MES team, maintain the incident queue in ServiceNow, lead Change Control activities, test new MES recipes, and generate validated documentation in line with GMP site

Qualifications

• Minimum 3–5 years' experience supporting IT applications and incident management in GMP environments.
• Experience implementing changes for IT applications with strong documentation and testing discipline.
• Ability to communicate effectively across multiple business and functional teams.

Responsibilities

• Maintain the incident queue in ServiceNow and resolve issues promptly.
• Initiate and lead Change Control activities.
• Develop and maintain well-documented configuration and deployment of MES recipes.
• Perform testing of new MES recipes and changes; generate validation documentation per GMP.
• Assist in incident investigations and ensure EHS procedures are followed.
• Support out-of-hours activities as the role evolves.

Skills

Troubleshooting IT apps

Change Control

Documentation

SQL

Visual Basic

Tools

MS SQL Server

VBScript/Visual Basic

Job description

Cognizant Ireland is seeking a Senior MES Recipe Author to implement System/MES recipe changes and manage day-to-day issues in the support of Electronic Batch Records, Weigh and Dispense, and Equipment Management modules on the Emerson Syncade MES solution at a large biotech facility in Cork.

You will operate in a collaborative MES team, maintain the incident queue in ServiceNow, lead Change Control activities, test new MES recipes, and generate validated documentation in line with GMP site