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Document Quality Control Specialist Contractor
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Full-time
- Job Overview: This role, for a Document QC Specialist Contractor, will manage the quality control of scientific documents and Bioanalytical data for the Translational DMPK and Clinical Pharmacology group.
- Conduct QC reviews of Bioanalytical data and study documents for compliance.
- Verify electronic lab notebook entries and adherence to Bioanalytical guidelines.
- Bachelors degree in a scientific or healthcare discipline with at least 4 years of experience in pharmaceuticals or biotech.
- Experience with LIMS/LabVantage and bioanalytical assays preferred, highlighting versatility in multi-tasking and sample management.
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