Deviations & Investigations Scientist

Eurofins · Columbia, MO

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Role summary

Eurofins BioPharm Services seeks a Deviations & Investigations Scientist to lead quality investigations, root cause analyses, and compliance documentation in a GMP-regulated laboratory environment. This intermediate-level role combines scientific expertise with technical writing and quality systems knowledge in a partially remote setting in Columbia, Missouri.

What they're looking for

Bachelor's degree in chemistry, biochemistry, biology, pharmaceutical sciences, or related field
1–3 years experience in cGMP-compliant laboratory settings
GLP and/or GMP experience with hands-on HPLC and/or GC knowledge preferred
LIMS system experience desirable
Strong organizational and communication skills with ability to manage multiple concurrent projects
Authorization to work indefinitely in the US without sponsorship

What you'll be doing

Lead and document laboratory investigations for deviations, OOS, OOT, and atypical quality events
Perform root cause analyses and support development and implementation of corrective and preventive actions
Review analytical data and laboratory documentation to validate investigation conclusions
Support stability testing and batch release programs through data review and quality assessments
Collaborate across laboratory, quality, and operational teams to resolve technical and compliance issues

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