Develop & validate PK & biomarker LBA methods to support pre-clinical & clinical studies. Independently perform manual & automated sample testing in GxP compliant manner by employing experience in using ELISA, MSD & appropriate software for data acquisition, analysis & presentation. Contribute to generation of test methods, validation plans & validation reports. Prepare buffers & reagents necessary for conducting assay runs. Document & archive data to ensure traceability & quality.
Requirements:
Must possess a Bachelor's in biology, microbiology, biochemistry or a highly related field of study, & 5 years developing bioanalytical methods & testing samples on ligand binding assay ("LBA") platforms. Alternatively, will accept a Master's degree in biology, microbiology, biochemistry or a highly related field of study, with 2 years work experience developing bioanalytical methods & test samples on LBA platforms.
Of experience required, must have 2 years in: (1) developing methods & test samples following Good Scientific/Clinical Practices (GxPs) guidelines; (2) performing manual & automated sample testing on LBA platforms including ELISA & MSD; (3) using automation systems & instrument software for assay steps, data acquisition & analyses; & (4) using PowerPoint, Word & Excel software & tools for data summary, plotting & presentations.
Work experience may be gained concurrently. Employer will accept any suitable combination of education, training or experience related to the job opportunity.
Application Instructions:
Apply online at https://careers.abbvie.com/en & reference REF38591F.
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