When you work as a Scientist I in the Mass Spec Bioanalysis Production group at KCAS, you get to further our mission by learning and applying your knowledge in bioanalytical and scientific principles to support regulated study execution under the guidance of senior scientists. You will build your foundation in GLP-compliant workflows, data integrity, and operational execution.
Our Mass Spec Bioanalysis Development team uses LC-MS/MS (Liquid Chromatography–Tandem Mass Spectrometry) techniques and sophisticated sample preparation methods to meet bioanalytical needs for drug discovery, preclinical, and clinical studies, including the bioanalysis of drugs and metabolites, biomarkers, and active endogenous compounds in biological fluids and tissues.
In this role, we will rely on you to:
- Execute regulated study activities including sample preparation and LC-MS/MS analysis under supervision
- Follow established methods and SOPs to ensure consistency and compliance in study execution
- Perform routine data processing and assist in preparing data summaries for review
- Maintain accurate documentation in compliance with study protocols, SOPs & GLP regulatory requirements
- Ensure proper sample identification, chain of custody, and data integrity
- Troubleshoot routine issues and escalate deviations appropriately
- Support audit readiness and adhere to quality and compliance standards
- Perform all aspects of the job in a way that supports company brand and supports company mission, vision, and values
To qualify specifically for this role, you will have:
- Bachelor’s or master’s in chemistry, Biochemistry or related field with 2+ years of experience in a laboratory environment
- Hands-on experience working in a GLP-regulated laboratory environment (required)
- Exposure to LC-MS/MS techniques and bioanalytical workflows
- Strong attention to detail and ability to work within SOP-driven and regulated environments
- Understanding of data integrity and compliance expectations in regulated studies