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Mes engineer - syncade

Cognizant Life Sciences Manufacturing
Engineer
Posted: 23h ago
Offer description

Cognizant is looking for dedicated, innovative and driven talent to join our expanding team in Cork. We’re currently looking for a full-time MES Engineer.
Responsibilities

Maintain the incident queue in Service Now and manage and resolve issues as they arise in a timely manner
Initiate and implement change control activities in accordance with quality standards and practices
Investigate and troubleshoot problems which occur and determine solutions or recommendations for changes and/or improvements
Prioritise support activities in line with project schedules

Qualifications

Minimum of 3 years of experience supporting IT applications, e.g. troubleshooting, managing incidents and change controls, design documentation, test case development, system and integration testing
Create business process flow diagram for pharmaceutical product recipes based on the paper batch record or source documents
Gather MES site specific requirement analysis to develop URS and FRS
Logically breakdown the recipes manufacturing process to configure the recipe in Werum PAS‑X
Develop/create MBR design elements (building blocks) and workflows in Werum PAS‑X for repetitive use in MBR creation to expedite the process
Gather master data and configure in Werum PAS‑X Development, Quality and Production Environment
Integrate Werum PAS‑X with SAP and other automation systems using standard interface component of MBR design
Lead the recipe design session with business process SMEs
Design MBR/recipe equipment workflow/status diagram based on the business process flow
Create solution design and configuration document
Prepare key user training documents and impart key user training
Provide assistance in business SOP creation
Hold a bachelor’s degree in Computer Science, Computer Engineering, Computer Information Systems or a related field (Technology Management, Chemical Engineering)
Have hands‑on experience with Werum PAS‑X product for full application configurations, including interface with SAP and automation systems
Have in‑depth knowledge of Bio‑pharma processes
Demonstrate the creation of business process flow diagrams
Possess knowledge of industry standards S88 and ISA S95
Understand pharmaceutical validation concepts
Be familiar with cGMP, GDP and GAMP standards

Benefits

You can pursue innovative career tracks and opportunities here
You can enhance your professional development through education and dedicated training
We’ll give you the skills you need to keep pace with the changing workplace while our compensation, benefits and wellness packages help you stay healthy and plan for the future

Additional Information

Employment type: Full‑time
Seniority level: Associate
Job function: Pharmaceutical Manufacturing

Please reach out to our friendly and welcoming team today to apply for this full-time hybrid MES Support Engineer position in Cork.
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