GMP Assessment Data Analyst
Role Overview
Weil Group is identifying specialists for potential assignments within a proposed pharmaceutical manufacturing quality-system assessment.
The opportunity depends on confirmed specialist scope, project award, and client confirmation.
The analyst supports reproducible cross-system checks and quantity or identity reconciliations using approved data under senior technical supervision.
Key Skills for This Role
Full Job Posting
Opportunity overview
Weil Group is identifying specialists for potential assignments within a proposed pharmaceutical manufacturing quality-system assessment.
The opportunity depends on confirmed specialist scope, project award, and client confirmation.
The analyst supports 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 GMP data-integrity and systems specialists.
Mandatory requirements
- Verifiable experience cleaning, joining, and reconciling structured data with traceable source and transformation records.
- Reproduce analytical results and document matching logic, assumptions, and exceptions.
- Handle confidential data and work under 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.
- 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 is desired.
- Relevant SQL, Python, R, or controlled Power Query expertise is desired.
- Experience reconciling ERP, MES, or laboratory data and working Spanish are desired.
Application and assignment terms
- Assignment scope, duration, and terms will be confirmed with selected consultants.
- Applicants are asked to provide project examples, location, availability for Manatí work, and a proposed hourly or daily consulting rate.
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