Senior MES Recipe Architect – Syncade (Hybrid)

Cognizant; Cork; Hybrid; EUR 60,000 - 90,000; Full time

Benefits offered by this job

Hybrid work model

Job summary

Cognizant in Cork, Ireland is seeking a Senior MES Recipe Author to implement System\MES recipe changes and manage day-to-day issues in support of Electronic Batch Records Weigh and Dispense and Equipment Management modules on our Emerson Syncade MES solution. The role is based at a large biotech facility in Cork with a hybrid work model.

You will join a collaborative MES team and work with cross-functional colleagues while ensuring GMP compliance and high-quality documentation.

Qualifications

• Experience maintaining incident queues and resolving IT issues.
• Experience implementing Change Control in GMP environments.
• Ability to document configurations clearly and maintainably.
• Experience testing MES recipes and changes.
• Experience generating validation documentation per GMP/site procedures.
• Knowledge of SQL and VB/VBA for MES configurations.

Responsibilities

• Maintain the incident queue in ServiceNow and resolve issues promptly.
• Initiate and implement Change Control activities per Quality Standards.
• Produce high-quality, well-documented configurations that are easily maintainable.
• Prioritize support activities in line with project schedules and test new MES recipes.
• Generate computer system validation documentation per site GMP guidelines.
• Follow EH&S procedures and assist in incident investigations.
• Collaborate across MES team and related stakeholders.

Skills

ServiceNow

Change control

GMP knowledge

MES experience

VB/VBA

SQL Server

Tools

MS SQL Server

Job description

Cognizant in Cork, Ireland is seeking a Senior MES Recipe Author to implement System\MES recipe changes and manage day-to-day issues in support of Electronic Batch Records Weigh and Dispense and Equipment Management modules on our Emerson Syncade MES solution. The role is based at a large biotech facility in Cork with a hybrid work model.

You will join a collaborative MES team and work with cross-functional colleagues while ensuring GMP compliance and high-quality documentation.