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We are looking for a dynamic, proactive, and talented person to join our team and perform the following tasks:
Responsibilities
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- 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
Technical Knowledge & Skills
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- Rockwell PharmaSuite
- Electronic Batch Records (EBRs)
- MES
- Microsoft Visio
- Process modeling
Qualifications
Years of experience: 6-8 years
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- 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
Working Conditions
Work schedule: 8:00 – 17:00. Permanent contract. xcskxlj
Benefits
Competitive salary and adaptable compensation plan adapted to your needs, including restaurant tickets, childcare tickets, transport tickets, and health insurance.
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📌 PharmaSuite MES Consultant (Madrid)
🏢 Tata Consultancy Services
📍 Madrid
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