Associate Scientist, Data Reviewer

Transpire BIO Inc.
  • Weston, FL
    2 days ago

    Job Description

    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.

    Numbers & Facts

    LocationWeston, FL

    Skills

    • Analysis Skillsunmatched
    • Blenderunmatched
    • Chemical Engineeringunmatched
    • Chemistryunmatched
    • Communication Skillsunmatched
    • Cross-Functionalunmatched
    • Data Qualityunmatched
    • Data Visualizationunmatched
    • Document Managementunmatched
    • Documentationunmatched
    • Documentation Reviewunmatched
    • English Languageunmatched
    • Forensic Scienceunmatched
    • High Performance Liquid Chromatography (HPLC)unmatched
    • Laboratoryunmatched
    • Laboratory Equipmentunmatched
    • Laboratory Techniquesunmatched
    • Manufacturing Equipmentunmatched
    • Manufacturing/Industrial Processesunmatched
    • Microsoft Excelunmatched
    • Microsoft PowerPointunmatched
    • Microsoft Wordunmatched
    • Multitaskingunmatched
    • Organizational Skillsunmatched
    • Pharmacyunmatched
    • Presentation/Verbal Skillsunmatched
    • Product Developmentunmatched
    • Project/Program Coordinationunmatched
    • Quality Assuranceunmatched
    • Quality Metricsunmatched
    • Record Keepingunmatched
    • Reporting Skillsunmatched
    • Research & Development (R&D)unmatched
    • Standard Operating Procedures (SOP)unmatched
    • Statisticsunmatched
    • Technical Writingunmatched
    • Time Managementunmatched
    • UV/VIS (Ultraviolet-Visible Spectroscopy)unmatched
    • Writing Skillsunmatched

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