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Associate Scientist, Data Reviewer

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Onsite

Associate Scientist, Data Reviewer

Transpire BIO Inc.

Associate Scientist, Data Reviewer

Skills

Testing & QARBlender

17 days ago

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Important information


Location:

Weston, FL, USA

Work mode:

Onsite

Published on:

6 October 2026

What they need


Job Summary

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.

Qualifications

  • 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.

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