Scientist I - Mass Spec Production (LC-MS/MS)
KCAS Bio
Summary
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.
Job description
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
Requirements
- Bachelor’s or master’s in chemistry, Biochemistry or 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
- Strong attention to detail
- Ability to work within SOP-driven and regulated environments
- Understanding of data integrity and compliance expectations in regulated studies
Benefits
- Company-Sponsored Events
- Career Development
- Stock Ownership Program
- Access to Latest Technology
- Paid Volunteer Time Off
Company overview
KCAS Bio is a leading global bioanalytical contract research organization (CRO) with over 45 years of experience in supporting drug development. Founded in 1979 and headquartered in Olathe, Kansas, the company provides comprehensive bioanalytical services from early discovery through clinical development and commercialization. With a team of approximately 375 employees and facilities across the United States, Europe, and Australia, KCAS Bio has supported the development of over 315 approved drugs and developed more than 6,200 proprietary and non-proprietary assays. The company specializes in biomarker testing, small and large molecule bioanalysis, immunogenicity testing, flow cytometry, molecular services, and clinical kitting. KCAS Bio maintains an exceptional regulatory compliance record, having successfully completed more than 20 FDA audits with no major findings. Their global presence and strategic alliances enable them to serve pharmaceutical and biotechnology clients worldwide with high-quality, GLP/GCP-compliant services that accelerate the development of life-changing therapies.