Project Role Description : Develop custom software solutions to design, code, and enhance components across systems or applications. Use modern frameworks and agile practices to deliver scalable, high-performing solutions tailored to specific business needs.

Must have skills : Manufacturing Engineering MES, communication skills verbal and written, microsoft excel

Good to have skills : NA

Minimum 3 Year(s) Of Experience Is Required

Educational Qualification : 15 years full time education

Summary: As a Pharmasuite MES Architect, you will be responsible for designing, developing template based MES recipes in Rockwell FactoryTalk PharmaSuite (FTPS) to support pharmaceutical manufacturing processes. You will collaborate with cross-functional teams to ensure efficient recipe authoring and seamless integration with automation and enterprise systems while adhering to regulatory and industry standards. Roles & Responsibilities: -Develop MES recipes using Rockwell FTPS, ensuring compliance with industry best practices. -Design and implement building blocks for reusable recipe structures. -Work closely with process engineers and manufacturing teams to map end-to-end pharmaceutical processes, with a focus on biologics. -Ensure compliance with pharmaceutical regulations (GMP, GxP, 21 CFR Part 11). -Participate in the full MES lifecycle, from design and validation to deployment and support. -Perform recipe testing, troubleshooting, and validation in alignment with SDLC (Software Development Life Cycle) methodologies. -Collaborate with DCS teams to ensure seamless MES-DCS integration for automated manufacturing. -Support and maintain MES systems in a validated state, ensuring high availability and performance. -Provide technical expertise in MES implementation and contribute to continuous improvements in manufacturing processes. Must-Have Skills: -MES experience in life sciences manufacturing, specifically with Rockwell FTPS. -Hands-on experience in MES-DCS integration for process automation. -Knowledge of ERP and Data Historian integration with MES. -Hands-on experience in recipe authoring, building block development, and validation. -Strong understanding of pharmaceutical manufacturing, especially biologics. Professional & Technical Skills: -Knowledge of SDLC and pharmaceutical regulations (GMP, GxP, 21 CFR Part 11). -Experience in executing at least one full MES lifecycle project with demonstrated results. -Good communication skills to collaborate with cross-functional teams. Additional Information: -Minimum 3 years of experience in MES recipe design and deployment in pharmaceutical manufacturing. -A full-time 15 years of education is required. -This position is based out of multiple locations., 15 years full time education