KCAS Bio

KCAS Bio

HQ
Olathe, Kansas
236 Total Employees
Year Founded: 1979

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Jobs at KCAS Bio

Search the 13 jobs at KCAS Bio

Recently posted jobs

Yesterday
Olathe, KS
Hybrid
Biotech
Responsible for global campaign management through digital platforms and channels, driving brand awareness and engagement. Create and manage marketing campaigns, optimize paid search and social ads, analyze consumer behaviors, oversee website strategies, and collaborate with the marketing team on growth strategies.
Biotech
Performing critical work in the Pharmaceutical Liquid Chromatography Mass Spectrometry (LC-MS/MS) lab, supporting regulatory submissions for drug discovery and clinical studies.
9 Days Ago
Olathe, KS
Hybrid
Biotech
The Contracts Manager at KCAS Bio is responsible for developing bids, proposals, and contracts for bioanalytical and biomarker projects. They also review contract terms, prepare budgets, and ensure compliance with service level agreements. Additionally, they collaborate with various departments to facilitate successful project execution.
Biotech
As an Analyst I on the Pharma LC-MS/MS team at KCAS Bio, you will process, prepare, analyze, and verify samples, contribute to client updates, and assist in basic experiment planning under the guidance of senior scientists. This role is ideal for new or recent graduates looking to kickstart their career in the scientific field.
Biotech
Design and execute bioanalytical projects, troubleshoot data, lead project teams, ensure compliance with protocols and regulatory requirements, communicate with clients, manage study timelines
Biotech
As a Sr Scientist at KCAS BioPharma LBA team, responsible for designing, planning, and executing bioanalytical assays, troubleshooting problems, leading scientific projects, and interacting with clients. Requires Bachelor's degree in related field and 4+ years of experience in large molecule immunoassay development/validation.
Biotech
As a Principal Scientist on the KCAS BioPharma LBA team, responsible for overseeing bioanalytical validations, providing scientific expertise, and leading research staff in protein quantitation and anti-drug antibody analysis using LBA, LCMS, and flow cytometry techniques.
Biotech
Seeking a Director of BioPharma Services at KCAS Bio in Olathe, KS. Responsible for leading and managing the Biopharma laboratory, developing workflow processes, and ensuring client deliverables meet expectations. Key roles include project management, strategic planning, business development, and maintaining client relationships. Must have experience in bioanalytical assays, immunoassay platforms, regulatory compliance, and team management.
Biotech
Lab Coordinator role in the Pharma LC-MS/MS group at KCAS Bio, responsible for supporting Pharma Operations personnel, maintaining laboratory equipment and supplies, ensuring regulatory compliance, and managing laboratory operations support staff.
Biotech
Lab Assistant role at KCAS Bio in the Pharma LC-MS/MS group, supporting timely completion of contracted services by providing specialized support. Responsibilities include checking reagents, preparing solutions, inventory management, equipment maintenance, and providing laboratory support. Requires an Associate's degree, experience with Scientific or LIMS software, knowledge of bloodborne pathogens and PPE, and regulatory experience (e.g., GLP). Previous work experience in a CRO is a plus.
Biotech
Performing critical work in Pharma LC-MS/MS lab using GLP and GCP methods to support regulatory submissions for drug discovery and clinical studies. Responsibilities include sample extraction techniques, method development, data interpretation, client interaction, and problem solving.
Biotech
As an Associate Scientist on the Pharma LC-MS/MS team at KCAS Bio, you will perform sample extraction techniques, method development using LC-MS/MS, interact with clients, and act as a technical expert. Requires a Bachelor's degree in Chemistry or related field with 1-3 years of industry experience.
Biotech
As a Report Coordinator Specialist at KCAS Bio, you will be responsible for accurately reporting pre-clinical and clinical bioanalytical data, creating data tables, and ensuring compliance with regulatory requirements. Additionally, you will assist in process improvement projects to enhance department efficiency.

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