Pharmaceutical Data Review Scientist

Eurofins USA BioPharma Services · Portage

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Company
Eurofins USA BioPharma Services
Location
Portage
Employment type
Full-time
Posted
October 16, 2026

About this job

Ensure that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations Review simple and complex routine and non-routine data (for three or more areas) according to departmental, corporate, and client SOPs; read and understand analytical procedures; ensure all work is performed according to GLP/GMP requirements and apply GLP/GMP in all areas of responsibility as appropriate Perform analysis of proteins and the impurities or raw materials associated with their production using various analytical techniques Determine if data is compliant and defendable based on industry regulations and methodology Verify data is of sound quality following all method, industry, and client requirements where applicable Diagnose problems,…

This is a short summary.

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