MES Recipe Author
Confirmed on the employer's own hiring board on Nov 10, 2026. First seen by Alion on Nov 10, 2026. Kstack scores B on the Alion truth index.
About the Role
We are seeking an experienced MES Recipe Author specializing in Emerson DeltaV Syncade to join a growing Manufacturing Execution Systems (MES) team supporting a large multinational biotechnology manufacturing facility.
The MES platform supports Electronic Batch Records (EBRs) and plays a critical role in maintaining efficient, reliable, and compliant manufacturing operations.
In this role, you will be responsible for designing, configuring, implementing, and supporting MES recipes at the manufacturing site. The ideal candidate has experience supporting IT applications, takes initiative, and is committed to developing a strong understanding of manufacturing processes and business needs.
Experience in pharmaceutical Active Pharmaceutical Ingredient (API) manufacturing is preferred.
Key Responsibilities
Develop, implement, configure, and support MES recipes using Emerson DeltaV Syncade.
Create high-quality, well-documented MES configurations that are reliable, maintainable, and aligned with operational requirements.
Collaborate with cross-functional site teams to configure, maintain, and support interfaces between MES and other systems, including ERP, automation, and laboratory systems.
Investigate and troubleshoot system issues, identify root causes, and recommend or implement corrective actions and process improvements.
Implement system design changes in accordance with established company quality standards and procedures.
Translate business and manufacturing requirements into technical designs, configurations, and MES recipes.
Develop and execute tests for new MES recipes, configuration updates, and system changes.
Prepare computer system validation (CSV) documentation in accordance with site procedures and Good Manufacturing Practice (GMP) requirements.
Maintain a strong commitment to quality, data integrity, and regulatory compliance in pharmaceutical manufacturing operations.
Work effectively with stakeholders across manufacturing, quality, engineering, IT, and other business functions.
Required Qualifications and Experience
Hands-on experience authoring MES recipes and working with the Emerson DeltaV MES (Syncade) platform.
3-5 years of experience supporting IT applications.
At least 2 years of experience working in a regulated environment.
3-5 years of hands-on experience in requirements gathering, design documentation, test case development, system and integration testing, commercial off-the-shelf (COTS) software implementations, and validation deliverables.
Strong understanding of the documentation, testing, and validation processes required in regulated manufacturing environments.
Excellent written and verbal communication skills, with a demonstrated ability to build effective working relationships across business and technical teams.
Proven ability to collaborate successfully with multiple business and functional teams.
Self-motivated, results-oriented, and able to work effectively both independently and as part of a team.
Preferred Qualifications
Experience in pharmaceutical API manufacturing operations.
Programming knowledge, particularly Visual Basic, with experience in configuration management and code deployment.
Experience with Microsoft SQL Server.
Ideal Candidate Profile
The ideal candidate combines hands-on MES recipe authoring expertise with a strong understanding of regulated manufacturing environments. They are proactive, detail-oriented, and focused on delivering high-quality technical solutions while maintaining rigorous quality and compliance standards.
Success in this role requires strong collaboration skills, technical ownership, and the ability to work effectively with stakeholders across manufacturing and technology teams.