Associate Scientist Mass Spec Production (LC-MSMS)
Kansas City, MO - USA
Job Summary
When you work as an Associate Scientist in the Mass Spec Bioanalysis Production group at KCAS you get to further our mission by applying your knowledge in bioanalytical and scientific principles to support regulated study execution with increasing independence. You will contribute to study activities from sample preparation through data generation while continuing to build your ability to assess data integrity and troubleshoot with guidance.
Our Mass Spec Bioanalysis Production team uses LCMS (Liquid Chromatography Mass Spectrometry) techniques to conduct bioanalytical testing in support of regulated preclinical and clinical studies including the quantification of drugs metabolites and biomarkers in biological matrices.
- Execute assigned study activities including sample preparation extraction and LCMS analysis with moderate supervision
- Perform established bioanalytical methods and procedures in support of regulated studies
- Perform data processing and prepare data summaries for review by senior scientific staff
- Troubleshoot routine sample preparation assay or instrumentation issues and escalate more complex challenges appropriately
- Maintain accurate and complete documentation in compliance with study protocols SOPs & GLP regulatory requirements
- Ensure proper sample identification handling tracking and chain of custody
- Support investigation and documentation of deviations or unexpected study results as needed
- Maintain laboratory and instrument readiness to support study execution and established timelines
- Communicate study progress issues and potential risks to senior staff
- Perform all aspects of the job in a way that supports company brand and supports company mission vision and values
- Bachelors or masters degree in chemistry Biochemistry Biology or related scientific field with 13 years of relevant laboratory experience
- Hands-on experience working in a GLP-regulated laboratory environment
- Experience with bioanalytical sample preparation and quantitative LC-MS/MS techniques
- Working knowledge of chromatographic principles and mass spectrometry
- Experience executing established bioanalytical methods in support of regulated studies
- Working knowledge of GLP documentation data integrity and sample handling requirements
- Ability to troubleshoot routine technical issues and recognize when escalation is necessary
- Strong attention to detail and ability to work effectively within SOP-driven and regulated workflows
Required Experience:
IC
About Company
As a full-service bioanalytical CRO and biomarker partner, KCAS Bio helps accelerate drug development in the pharma and biopharma industries with large and small molecule bioanalysis.