Associate Scientist, Data Reviewer

Transpire BIO Inc. • Weston, FL

6d

About The Position

The Associate Scientist, Data Reviewer conducts data review and data-integrity verification before R&D data records are submitted to QA for review and release. The role leads data verification and documentation review, drafts summary reports and visualizations of laboratory data, and maintains and uploads R&D documents in document management systems. Activities are performed in accordance with Standard Operating Procedures (SOPs), while meeting technical and quality standards.

Requirements

• Bachelor of Science degree, preferably in chemistry, chemical engineering, pharmacy, forensic sciences, or a related field.
• At least 3 years of work experience in a cGMP-regulated environment in a relevant discipline.
• Familiarity with analytical methodology, laboratory practices, wet chemistry, and laboratory equipment such as HPLC/UPLC, UV-Vis, and GC.
• Strong organizational skills and ability to manage multiple priorities and deadlines in a fast-paced environment.
• Proficiency in Microsoft Excel, Word, and PowerPoint.
• Written and verbal communication skills in English.

Nice To Haves

• Familiarity with manufacturing or manufacturing-process equipment used in laboratories, such as liquid manufacturing equipment and powder blenders.
• Experience with document management systems.
• Experience with statistical analysis applications.

Responsibilities

• Lead the organization, maintenance, and control of documentation and records for R&D product development activities.
• Conduct technical document reviews and data verification, and prepare reports and visual summaries.
• Ensure the integrity and accuracy of documents and data before submitting 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 applicable company policies, procedures, and quality requirements.
• Conduct activities following Standard Operating Procedures and ensure technical and quality standards are met.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level