Custom Software Engineer

Project Role :Custom Software Engineer

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

Good to have skills :NA

Minimum 15 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 15 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.

Qualification 15 years full time education