GMP Assessment Data Analyst at Weil Group
Manati, PR Biotech/Pharmaceutical — full-time
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