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# Associate Scientist, Data Reviewer

- **Company:** Transpire Bio
- **Location:** Weston, FL, United States
- **Experience:** Experienced
- **Contract:** Contract
- **Skills:** Microsoft Word, Microsoft Excel, Data Validation, Data Integrity, Document Management Systems, Microsoft PowerPoint
- **Published:** October 4, 2026
- **Apply:** https://www.indeed.com/viewjob?jk=0741a669268bb765

## About the Role

* BS Degree preferably in chemistry, chemical engineering, pharmacy, forensic sciences or related fields.
 * 3+ years of work experience in cGMP regulated environment in the relevant discipline is a must to have.
 * Familiarity with analytical methodology, laboratory practices, wet-chemistry, equipment used in laboratories such as HPLC/UPLC, UV-Vis, GC etc.
 * Familiarity with manufacturing or manufacturing process equipment used in laboratories such as liquid manufacturing equipment, powder blender etc. is a plus.
 * Strong organizational skills, with the ability to manage multiple priorities and deadlines in a fast-paced environment.
 * Proficiency in Microsoft Excel, Word, and PowerPoint, is a must to have.
 * Experience with document management systems is a plus.
 * Experience with statistical analysis applications in a plus.
 * Written and verbal communication skills in English is a must to have.

## Description

Conducts data review and data integrity verification prior to submission of R&D data records to QA for review and release. Leads data verification, documentation review, drafts summary reports, and drafts visualization of data from the laboratories. Maintains and uploads R&D documents in document management systems. Conducts activities following Standard Operating Procedures (SOPs). Assures that Technical and Quality standards are met.
Essential Duties and Responsibilities

 * Lead the organization, maintenance, and control of documentation and records for R&D product development activities.
 * Responsible for technical review of documents, data verification, and preparation of reports and visual summaries.
 * Responsible for ensuring data integrity and accuracy of documents and data prior to submission of R&D data records to QA for review and release.
 * Maintain and upload R&D documents in document management systems.
 * Coordinate routine project activities, documentation, materials, and communications with internal teams and external partners.
 * Participate in meetings, maintain accurate records, and follow up on assigned actions.
 * Support project timelines and contribute proactively to team objectives.
 * Build and maintain effective working relationships with cross-functional colleagues and external partners.
 * Perform other duties as assigned and comply with all applicable company policies, procedures, and quality requirements.