Sr. Scientist - LC-MS/MS Bioanalysis (Sample Analysis)
When you work as a Senior Scientist in the Mass Spec Bioanalysis Production group at KCAS, you get to further our mission by applying your extensive scientific expertise to provide technical leadership and oversight of complex LC-MS/MS sample analysis activities. You will guide study execution, resolve challenging analytical issues, ensure scientific quality and data integrity, and mentor junior scientists while supporting study timelines, regulatory compliance, and successful delivery of high-quality bioanalytical results.
Our Mass Spec Bioanalysis Production team uses LC-MS/MS (Liquid Chromatography–Tandem Mass Spectrometry) techniques and established bioanalytical methods to perform sample analysis in support of preclinical and clinical studies. Our work focuses on generating accurate, reliable, and high-quality bioanalytical data while maintaining compliance with applicable regulatory requirements and laboratory procedures.
In this role, we will rely on you to:
- Execute and oversee all phases of assigned studies including sample preparation, LC-MS/MS analysis, data review, and report generation in a regulated environment
- Act as lead scientist on studies, providing work direction, technical guidance, and training to junior scientific staff
- Be responsible for all client communication related to study conduct and data delivery
- Interact with QAU to resolve audit findings, deviations, and compliance-related issues
- Have final authority for sample identification, including resolution of discrepancies with clinical sites and/or clients
- Be accountable for study timelines, deliverables, and communication of status to management and clients
- Ensure compliance of all study activities with study protocols, SOPs & GLP regulatory requirements
- Review and ensure accuracy, completeness, and integrity of data prior to reporting
- Support audit readiness and participate in client and regulatory inspections as needed
- Act as a technical resource for troubleshooting assay performance and operational challenges within a production environment
- 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, Master’s, or PhD in Chemistry, Biochemistry, or related field with at least 5 years of experience in a bioanalytical laboratory environment
- Extensive hands-on experience working in a GLP-regulated laboratory environment (required)
- Strong experience with bioanalytical sample preparation and quantitative LC-MS/MS workflows
- Experience executing regulated studies, including data review, reporting, and audit support
- Demonstrated ability to troubleshoot technical and operational issues in a production environment
- Experience interacting with Quality Assurance and supporting audits and inspections
- Prior experience acting as a study lead or Principal Investigator–type role preferred
Source: the employer's careers page. Last checked 2026-11-06. Posted 2026-10-28.
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