GMP Systems Integration Architect — Manufacturing Data & Genealogy

Weil Group, Inc; United States; Hybride; USD 100 000 - 150 000; Plein temps

Résumé du poste

Weil Group Inc. is seeking qualified consultants for a pharmaceutical manufacturing quality-system assessment on a project basis, subject to award and client confirmation.

Assess how lot identifiers, quantities, status and data meaning are preserved across GMP systems and how failed or inconsistent hand-offs are detected and reconciled. This engagement requires on-site work in Manat, Puerto Rico, with approved remote work where appropriate.

Qualifications

• Experience assessing or integrating data flows between GMP manufacturing, materials, laboratory or quality systems.
• Ability to trace a real transaction through at least two critical systems and verify identifiers, quantities, units, status and timing.
• Hands-on analysis of failed messages, duplicates, retries, timing differences, reconciliation and exception controls.
• Connect interface failures with materials genealogy or release evidence and assess controls and validation documentation.
• Work directly with system owners, IT, automation and operations stakeholders.
• Professional English for technical records, deliverables and stakeholder discussions.
• On-site work in Manat, Puerto Rico with approved remote work where appropriate.
• Confidentiality, site and information-handling requirements.

Responsabilités

• Map actual interfaces between manufacturing, materials, laboratory and quality systems.
• Follow transactions across sources and receiving systems, including manual bridges and exceptions.
• Recommend feasible reconciliation, monitoring and error-handling controls that support genealogy and release.

Connaissances

Data integration

GMP systems

System interfaces

Stakeholder collaboration

Formation

Engineering degree or equivalent

Outils

ERP/MRP

MES

LIMS

eQMS

Description du poste

Weil Group Inc. is seeking qualified consultants for a pharmaceutical manufacturing quality-system assessment on a project basis, subject to award and client confirmation.

Assess how lot identifiers, quantities, status and data meaning are preserved across GMP systems and how failed or inconsistent hand-offs are detected and reconciled. This engagement requires on-site work in Manat, Puerto Rico, with approved remote work where appropriate.