When you work as a Scientist 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 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.
In this role, we will rely on you to:
- Execute regulated study activities including sample preparation and LCMS 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 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
Skills Required
- Bachelor's or master's in chemistry or a related field
- 2+ years of experience in a laboratory environment
- Hands-on experience working in a GLP-regulated laboratory environment
- Exposure to LC-MS/MS techniques and bioanalytical workflows
What We Do
With its presence in three locations across North America and Europe, KCAS Bio is a leading contract research organization (CRO) employing top scientific talent and providing comprehensive bioanalytical services to the global biopharmaceutical industry from early discovery support through product registration and beyond. The collaboration of the three entities allows for global support in bioanalytical, biomarker, immunogenicity, cellular and molecular assay services along with clinical kitting and sample management. The KCAS family of companies operates in state-of-the-art facilities in the United States and Europe. This business structure enables the expertise, capacity, and flexibility to support the development of all types of drugs, biologics, cell and gene therapies to improve health worldwide. Our purpose is to help accelerate the discovery and development of life-changing drugs smoothly, safely and sustainably.
