MES Engineer - Rockwell PharmaSuite MES Engineer - Rockwell PharmaSuite

MES Engineer - Rockwell PharmaSuite

Full Time • MES Engineer - Rockwell PharmaSuite
This is a fully onsite role from day 1. NO remote option.

W2/C2C 

This assignment will encompass the development of MES recipes and workflows as specified by solution architects through formal and customer-approved documentation such as User Requirements Specifications (URS), Software Design Specifications (SDS), and Functional Specifications (FS) to build the Electronic Batch Record as per the client’s manufacturing process within the scope of the project.


Job Duties:
  • Coordinate with stakeholders and project leads within the development team to ensure timely delivery of building blocks, EBRs, and new releases, and implement the Rockwell FTPS MES Plan while overseeing project lifecycle management.
  • Author recipes and workflows as per requirements to deliver the EBR
  • Develop and collaborate on the MES Roadmap, addressing lifecycle upgrades, global and business standards, cutover plans, and providing technology guidance.
  • Maintain MES configuration and Master Data to ensure data integrity and GMP compliance, and authored recipes, SOPs, URS/FRS, and process mapping documents.
  • Recipe and Workflow Authoring: Read, understand, and configure recipes and workflows as per provided URS and design documentation, and provide feedback to solutions architects and project managers regarding errors, omissions, and solutions improvements as needed.
  • Data Configuration: Map OPC/Live data between MES and customer automation systems as required to configure Data Manager and to achieve the EBR solution.
  • Peripheral Configuration: Support the configuration of peripheral devices such as weighing scales, printers, barcode scanners, flatbed scanners, and similar devices necessary to achieve the EBR requirements.
  • Solution specification and documentation: collaborate with client resources as needed to interpret and update user, functional, and system requirements specifications to ensure the end solution reflects the client’s requirements, deliver the proposed value and help enforce vendor accountability.
Qualifications:
  • 10 + industry experience with 3-5 years of experience as a Rockwell PharmaSuite MES Engineer doing system configuration, recipe, and workflow development, and supporting validation/qualification efforts in heavily regulated environment within the life sciences.
  • Must have prior experience developing EBR solutions and interfacing with automation systems.
  • Bachelor’s degree in engineering, computer science or related, required.




(if you already have a resume on Indeed)

Or apply here.

* required fields

Location
Or
Or