Are you a PharmaSuite MES Consultant in Madrid, Spain seeking a new interesting challenge? ?

If your answer is yes, it’s your lucky day so keep reading, it can be just what you're looking for ?

✍️ WHAT WILL YOU DO?
We are looking for a dynamic, proactive and talented person to join our team and perform the following tasks:
- Participate in fit-gap analysis, process modeling and process standardization activities with process leads and SMEs
- Work with lead resources to develop Building Block requirements
- Provide effort estimates, user story point estimates and status updates for assigned stories
- Author and execute validation-related documentation for Electronic Batch Records (EBRs)
- Configure EBRs across Development, Stage and Production environments
- Address site-specific questions, use cases and enhancement requests
- Collaborate with multiple teams to gather and define requirements for development activities
- Provide HyperCare and Go-Live support

? WHAT TECHNOLOGIES, METHODOLOGIES OR TOOLS WILL YOU USE?
- Rockwell PharmaSuite
- Electronic Batch Records (EBRs)
- MES




- Microsoft Visio
- Agile methodologies
- Requirements authoring
- Validation documentation
- Process modeling

? WHAT ARE WE LOOKING FOR?
Years' experience: 6-8 years
English: C1
- Understanding of pharmaceutical manufacturing processes (solid oral dose and packaging preferred)
- Expertise in Good Documentation Practices and Good Testing Practices
- Ability to convert paper batch records into PharmaSuite EBRs
- Ability to migrate legacy EBRs into PharmaSuite using existing functionality
- Ability to design reusable Building Blocks
- Ability to author requirements, specifications and validation documents
- Ability to test EBR functionality in a compliant manner
- Ability to work in a fast-paced agile team environment

? WHERE AND WHEN?
Workplace: On-site — Alcobendas, Spain
Work Schedule: 8:00 – 17:00

? WHAT CAN WE OFFER YOU?
Permanent contract ? - We offer indefinite contracts from the firs

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