GMP Assessment Data Analyst

Weil Group, Inc; Manatí (PR); Hybrid; USD 60,000 - 90,000; Full time

Job summary

Weil Group Inc. is seeking specialists to support pharmaceutical manufacturing quality-system assessments in Manatí, Puerto Rico, with supervision from senior technical reviewers.

The role emphasizes preparing data extracts, tracking data lineage, and delivering reproducible outputs for GMP data-integrity specialists. On-site availability with approved remote work where appropriate is required.

Qualifications

• Typically 3 or more years of directly relevant professional experience.
• Practical spreadsheet and database-query or equivalent analytical skills.
• Understanding of controlled records, versioning and GMP data-handling expectations.
• Relevant analytical, information-systems, engineering or scientific education, or equivalent experience.

Responsibilities

• Prepare approved data extracts for documented comparisons and reconciliations.
• Track source files, versions, transformations, matching keys and exceptions.
• Provide reproducible analytical outputs for interpretation by GMP data-integrity specialists.

Skills

Data reconciliation

Data cleaning

SQL

Python

Power Query

Education

Bachelor's degree in a related field

Tools

SQL

Python

Job description

Weil Group Inc. is identifying specialists for potential assignments within a proposed pharmaceutical manufacturing quality-system assessment. This opportunity is subject to confirmed specialist scope, project award and client confirmation.

Support reproducible cross-system checks and quantity or identity reconciliations using approved data under senior technical supervision.

What you will do

• Prepare approved data extracts for documented comparisons and reconciliations.
• Track source files, versions, transformations, matching keys and exceptions.
• Provide reproducible analytical outputs for interpretation by the GMP data-integrity and systems specialists.

Mandatory requirements

• Verifiable experience cleaning, joining and reconciling structured data with traceable source and transformation records.
• Ability to reproduce analytical results and document matching logic, assumptions and exceptions.
• Disciplined confidential-data handling and willingness to work under the designated senior technical reviewers.
• 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 3 or more years of directly relevant professional experience, or a demonstrably equivalent track record.
• Practical spreadsheet and database-query or equivalent analytical skills for quantities, units, identifiers and statuses.
• Understanding of controlled records, versioning and relevant GMP data-handling expectations.
• Relevant analytical, information-systems, engineering or scientific education, or equivalent practical experience.

Desired qualifications

• Prior pharmaceutical, manufacturing or other regulated-data experience.
• Relevant SQL, Python, R or controlled Power Query expertise.
• Experience reconciling ERP, MES or laboratory data and working Spanish.

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