Jobs at KCAS Bio

Supports quality assurance for bioanalytical work by reviewing documents, data, protocols, and reports; conducting audits and inspections; reviewing deviations and investigations; maintaining QA records; assisting with SOP reviews, training, data trending, and continuous improvement. Collaborates with scientific and operational teams to ensure regulatory, procedural, and quality compliance while managing multiple priorities accurately and professionally.

Lead regulated bioanalytical studies from setup through reporting using LC-MS/MS and sample preparation workflows. Perform data review, troubleshoot assay and production issues, ensure GLP compliance and data integrity, communicate with clients, resolve audit findings with Quality Assurance, oversee study timelines, and train junior staff. Support audit readiness and regulatory inspections while serving as a technical and study lead.

Coordinates the preparation, review, formatting, validation, and finalization of scientific study reports for bioanalytical studies. Compiles report sections and data tables, identifies discrepancies, ensures compliance with protocols, SOPs, GLP requirements, and regulatory standards, tracks deadlines, maintains documentation, and collaborates with scientists and study teams. The role also supports templates, process improvements, reporting technology updates, and junior team members.

Execute bioanalytical ligand binding assays supporting drug discovery, preclinical, and clinical studies. Responsibilities include sample and reagent preparation, assay execution, method development and validation support, data processing, troubleshooting, GLP-compliant documentation, sample tracking, and communicating study progress. The role requires increasing independence while providing informal guidance to junior staff.

Conduct molecular bioanalytical method development, validation, and sample analysis in a GLP-regulated laboratory. Perform PCR, qPCR, ddPCR, nucleic acid extraction and quantification, cell culture, and work with human blood, primary cells, and tissues at BSL-II. Plan experiments, analyze and interpret data, review documentation, troubleshoot technical issues, maintain equipment, support SOPs and reports, train junior staff, and manage multiple study timelines.

Perform supervised bioanalytical studies using LC-MS/MS, including sample preparation, method development, analysis, data processing, troubleshooting, documentation, and sample tracking. The role supports drug discovery, preclinical, and clinical research involving drugs, metabolites, biomarkers, and endogenous compounds. Scientists will apply chromatographic and mass spectrometry principles, maintain regulatory compliance, communicate progress, and escalate issues to senior staff.

Supports mass spectrometry bioanalysis laboratory operations by maintaining cleanliness, supplies, bulk solutions, equipment readiness, safety, and documentation. Performs routine equipment checks and maintenance, assists with plate washer operation, follows SOPs and GLP requirements, and ensures scientists have the materials and operational support needed for drug discovery, preclinical, and clinical bioanalytical studies.

The Sr. Scientist in Mass Spec Development will lead bioanalytical projects, design experiments, conduct method development, and ensure compliance with study protocols and regulatory requirements.

Develop and grow strategic relationships across assigned life sciences key accounts, expand adoption of bioanalytical and biomarker services, achieve booking and revenue targets, manage account plans and pipelines, negotiate complex opportunities, and coordinate with scientific, operational, marketing, and program management teams. The role requires understanding CRO sales cycles, client pipelines, technical service offerings, and regulated bioanalytical environments.

The Director of Quality Assurance at KCAS Bio oversees QA departments, manages quality systems, leads regulatory audits, and interacts with executive management and clients to ensure compliance and high-quality standards in bioanalytical services.

Serve as a technical lead for bioanalytical validations and biostudies, overseeing method development (LBA, LCMS, immunoassays), supervising staff, reviewing and reporting study results, mentoring scientists, troubleshooting assays, ensuring GLP/SOP compliance, and interfacing with sponsors and subcontractors to integrate and deliver high-quality study outcomes.

Remote Director of Business Development responsible for achieving territory sales goals in the Mid-Atlantic, prospecting and closing complex bioanalytical service contracts, managing accounts in Salesforce/HubSpot, developing proposals/SOWs, representing KCAS at conferences, and maintaining technical expertise across LC-MS/MS, ligand binding, flow cytometry, and molecular platforms within GLP/GCP environments. Requires significant client-facing interaction and travel (25-40%).

Perform bioanalytical LC‑MS/MS testing for regulated preclinical and clinical studies: sample preparation, extraction, LCMS analysis, data processing, documentation under GLP, troubleshoot routine issues, maintain instrument readiness, and communicate with senior staff.

As a Sr. Scientist at KCAS Bio, you will lead bioanalytical studies from setup to reporting, utilize your expertise in ligand binding assays, ensure compliance with GLP standards, and support client communications while mentoring junior scientists.