Senior GMP Systems Integration and Manufacturing Data Architect

Weil Group, Inc.; Puerto Rico; Hybrid; USD 90,000 - 130,000; Full time

Job summary

Weil Group Inc. is seeking a qualified consultant to map interfaces between manufacturing, materials, laboratory and quality systems and to trace transactions across key systems. The project focuses on reconciliation, monitoring and error-handling controls supporting genealogy and release.

The engagement is project-based, on-site in Manatí, Puerto Rico, with approved remote work where appropriate. Ideal candidates have 7+ years of directly relevant experience, and strong knowledge of ERP/MRP,

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.

Responsibilities

• Map interfaces between manufacturing, materials, laboratory and quality systems.
• Trace transactions across sources and receiving systems; follow data lineage.
• Recommend reconciliation, monitoring and error-handling controls that support genealogy and release.

Skills

Data flow mapping

GMP systems knowledge

ERP/MRP/MES/LIMS/eQMS familiarity

Stakeholder collaboration

Education

Engineering or information systems degree

Tools

ERP/MRP

MES

LIMS

eQMS

Job description

Weil Group Inc. is identifying qualified consultants for a proposed pharmaceutical manufacturing quality-system assessment. This project-based opportunity is subject to project award and client confirmation.

What you will do

• 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.

Mandatory requirements

• Verifiable 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.
• Ability to connect interface failures with materials genealogy or release evidence and assess controls and validation documentation.
• Ability to work directly with system owners, IT, automation and operations stakeholders.
• Professional English for technical records, deliverables and stakeholder discussions.
• Availability for assigned on-site work in Manatí, Puerto Rico, with approved remote work where appropriate.
• Ability to meet confidentiality, site and information-handling requirements and disclose potential conflicts affecting independent assessment.

Necessary qualifications

• Typically 7 or more years of directly relevant professional experience, or a demonstrably equivalent track record.
• Functional understanding of ERP/MRP, MES, LIMS, eQMS and warehouse systems; interpret maps, configurations and transaction logs.
• Reproducible analysis of approved data extracts or queries, and design of reconciliation and monitoring controls.
• Relevant education in engineering, information systems, automation or equivalent regulated-systems experience.

Desired qualifications

• Hands-on experience with the platforms, versions and interfaces confirmed for the project.
• Knowledge of automation, historians and equipment-to-batch data relationships.
• Complex genealogy, controlled migrations or multi-platform reconciliation projects.

Weil Group is proud to be an Equal Employment Opportunity Employer.