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 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
About Accenture Accenture is a leading global professional services company that helps the world's leading businesses, governments and other organizations build their digital core, optimize their operations, accelerate revenue growth and enhance citizen services--creating tangible value at speed and scale. We are a talent- and innovation-led company with approximately 791,000 people serving clients in more than 120 countries. Technology is at the core of change today, and we are one of the world's leaders in helping drive that change, with strong ecosystem relationships. We combine our strength in technology and leadership in cloud, data and AI with unmatched industry experience, functional expertise and global delivery capability. Our broad range of services, solutions and assets across Strategy & Consulting, Technology, Operations, Industry X and Song, together with our culture of shared success and commitment to creating 360 value, enable us to help our clients reinvent and build trusted, lasting relationships. We measure our success by the 360 value we create for our clients, each other, our shareholders, partners and communities.
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