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 7.5 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.
• Solid 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 8 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.

📌 Custom Software Engineer (Pune)
🏢 Accenture in India
📍 Pune