**Requirements**:
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 lead RA 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
**Job Type**: Contract
Contract length: 12 months
Work Location: Hybrid remote in 63100 ASCOLI PICENO, AP
📌 Ftps Recipe Authors
🏢 Siro Clinpharm
📍 Ascoli Piceno