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Scientist, Data Review

Columbia, MO, us💼 Full-time🗓 2026-07-21 → 2026-07-31

Core

Review scientific reports under cGMP guidelines to ensure regulatory compliance, data accuracy, and report quality in a laboratory setting.

Role type

Associate Scientist (Quality Assurance)

Builds

High-quality scientific reports for pharmaceutical and life sciences clients

Domain

Pharmaceutical / Life Sciences / Quality Assurance

Deliverable

production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work

Required skills

cGMP compliance knowledge, laboratory experience, data accuracy verification, report sign-off authority, internal audit assistance, protocol adherence

Preferred skills

GMP pharmaceutical setting experience, strong organizational skills, ability to follow direction, attention to detail, independent work capability

Technologies

Laboratory protocols, Standard Operating Procedures (SOPs)

Responsibilities

Review scientific reports for regulatory compliance and data accuracy, assist with internal audits, collaborate with lab operations staff, perform final report sign-off

Seniority

Entry-level

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