- Understanding of pharmaceutical manufacturing processes (Solid oral dose and packaging preferred)

- Possesses expertise in Good Documentation and Good Testing Practices

- Ability to process map site requirements using Microsoft Visio or alike software

- Ability to work with site SMEs to turn paper batch records into EBRs in Rockwell Pharmasuite utilizing existing functionality

- Ability to work with site SMEs to turn existing EBRs in legacy systems (P2C2, PMX, etc.) into Rockwell Pharmasuite EBRs utilizing existing functionality

- Ability to design Building Blocks that can be reused in multiple processes

- Ability to author requirements, SPEC, and validation documents

- Ability to test an EBR full functionality in a compliant manner

- Ability to work in a fast paced agile team environment

Roles & Responsibilities :

- Participates in fit gap analysis & Process Modeling & process standardization with Area lead & Process SME

- Works with Rockwell Automation Lead to develop BB requirements

- Provide times, user story point estimates, and status for all stories assigned to them

- Authors and performs documents supporting validation of EBRs

- Configures EBR in Development, Stage, & Production Environment

- Address Site specific questions, use cases and ER from Site EBR and PO

- Works across the teams to put requirement together for ER development

- Provide HyperCare and Go-live support