¡Nueva! Se el primero en solicitar

MES Recipe Author

MES Recipe Author for pharmaceutical manufacturing processes (Solid oral dose and packaging preferred)Algete, Community of Madrid, Spain6-12 Month contracrHybrid

Descripción del empleo

MES Recipe Author for pharmaceutical manufacturing processes (Solid oral dose and packaging preferred)

Algete, Community of Madrid, Spain

6-12 Month contracr

Hybrid Mode


Your responsibilities:

  • Execution and coordination of responsibilities that include Master Recipe creation, master data creation, maintenance and control of MES activities (Recipe and workflow designer, PMC, PEC, PRC and Data manager Clients).
  • Process mapping (visio), Recipe designing, Testing, Dry runs and Business verification of the created recipes.
  • Understanding of pharmaceutical manufacturing processes (Solid oral dose and packaging preferred)
  • Possesses expertise in Good Documentation and Good Testing Practices
  • Building, Testing and verifying of recipes which require Integration (SAP, gLIMS, catalyst etc).
  • Coordination with core and site teams for new site-specific requirements.
  • 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 work in a fact paced agile team environment
  • Preparing and conducting UAT, Change management, Validation Documentation, User training


Your Profile

Essential skills/knowledge/experience: (Up to 10, Avoid repetition)

  • Expert in PharmaSuite and specific functionalities.
  • 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
  • Experience: 9+ Years

Información extra

Status
Activa
Estudios requeridos
E.S.O
Localización
Madrid
Tipo de contrato
Trabajo estudiantes
Publicado el
13-02-2026
Carnet de conducir
No
Vehículo
No
Carta de motivación
No
Idiomas
Español

Madrid | Trabajo estudiantes | E.S.O

Solicita ya

Compartir esta oferta