GMP Assessment Data Analyst
Weil Group
1 day ago
On-site
Puerto Rico, United States
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.
**Weil Group is proud to be an Equal Employment Opportunity Employer.**
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.
How to apply
Apply through this posting with your CV, relevant project examples, current location, availability for work in Manatí and proposed hourly or daily consulting rate. Assignment scope, duration and terms will be confirmed with selected consultants.**Weil Group is proud to be an Equal Employment Opportunity Employer.**