MES Recipe Author

Cognizant Technology Solutions Corporation; Cork; On-site; EUR 60,000 - 90,000; Full time

Job summary

Cognizant is seeking an MES Recipe Author to join a growing MES team at a life science manufacturing site in Cork. You will design, configure, test, and support DeltaV MES (Syncade) recipes for Electronic Batch Records in line with GMP and company quality standards.

You will collaborate with site teams on ERP automation and laboratory interfaces, produce well-documented recipe configurations, perform testing, and contribute to validation deliverables while upholding data integrity and strong

Qualifications

• Experience in MES recipe authoring and knowledge of Emerson DeltaV MES (Syncade).
• 3 to 5 years of experience supporting IT applications.
• Minimum of 2 years of experience in a regulated environment.
• 3 to 5 years of hands-on experience in requirements gathering design documentation test case development system and integration testing COTS implementations and validation deliverables.
• Programming and Visual Basic knowledge with configuration management and deployment experience is advantageous.
• MS SQL Server experience is an advantage.
• Pharmaceutical API manufacturing experience is desirable.
• Strong communication skills with a proven ability to build cross-functional relationships.

Responsibilities

• Design develop implement and support DeltaV MES (Syncade) recipes for Electronic Batch Records in a life science manufacturing environment.
• Produce high-quality well-documented and easily maintainable recipe configuration.
• Translate business and manufacturing requirements into recipe designs and carry out testing of new recipes and changes.
• Collaborate with site teams to configure and support interfaces between MES and other systems including ERP automation and laboratory systems. Investigate and troubleshoot issues then determine solutions and recommend changes or improvements.
• Implement system design changes in accordance with company quality standards practices and change control procedures.
• Generate computer system validation documentation including requirements design specifications test cases and test reports in line with site procedures and GMP guidelines.
• Perform system and integration testing supporting COTS implementations and validation deliverables.
• Manage configuration and deployment of developed code using Visual Basic and MS SQL Server knowledge where applicable.
• Uphold data integrity and the importance of the quality control function in pharmaceutical production and act with a high level of integrity at all times.
• Build strong working relationships within the MES team and across business and functional teams communicating clearly in both written and verbal form.
• Work independently and as part of a team taking ownership of deliverables and developing a solid understanding of the business and its API manufacturing operations.

Skills

MES recipe authoring

DeltaV Syncade

Regulated environment

IT applications support

Visual Basic

MS SQL Server

Pharma API experience

Communication skills

Tools

Visual Basic

MS SQL Server

Job description

MES Recipe Author

• Join a growing MES team supporting Electronic Batch Records at a large multi-national biotech manufacturing site in Cork.

• As an MES Recipe Author you will design configure test and support DeltaV MES (Syncade) recipes in line with GMP and company quality standards.

• You will partner with site teams on ERP automation and lab system interfaces and you will bring a self-motivated delivery-focused approach to the role.

Responsibilities :

• Design develop implement and support DeltaV MES (Syncade) recipes for Electronic Batch Records in a life science manufacturing environment.

• Produce high-quality well-documented and easily maintainable recipe configuration.

• Translate business and manufacturing requirements into recipe designs and carry out testing of new recipes and changes.

• Collaborate with site teams to configure and support interfaces between MES and other systems including ERP automation and laboratory systems. Investigate and troubleshoot issues then determine solutions and recommend changes or improvements.

• Implement system design changes in accordance with company quality standards practices and change control procedures.

• Generate computer system validation documentation including requirements design specifications test cases and test reports in line with site procedures and GMP guidelines.

• Perform system and integration testing supporting COTS implementations and validation deliverables.

• Manage configuration and deployment of developed code using Visual Basic and MS SQL Server knowledge where applicable.

• Uphold data integrity and the importance of the quality control function in pharmaceutical production and act with a high level of integrity at all times.

• Build strong working relationships within the MES team and across business and functional teams communicating clearly in both written and verbal form.

• Work independently and as part of a team taking ownership of deliverables and developing a solid understanding of the business and its API manufacturing operations.

Key Requirements

• Experience in MES recipe authoring and knowledge of Emerson DeltaV MES (Syncade).

• 3 to 5 years of experience supporting IT applications.

• Minimum of 2 years of experience in a regulated environment.

• 3 to 5 years of hands-on experience in requirements gathering design documentation test case development system and integration testing COTS implementations and validation deliverables.

• Programming and Visual Basic knowledge with configuration management and deployment experience is advantageous.

• MS SQL Server experience is an advantage.

• Pharmaceutical API manufacturing experience is desirable.

• Strong communication skills with a proven ability to build cross-functional relationships.

Cognizant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.