Scientist I - Mass Spec Production (LC-MS/MS, GLP)

Performing critical work that impacts our industry and our world’s health while problem solving and innovating in the field – that is what Scientists at KCAS Bio get to do every day. If that gets you excited too, then maybe working as a Scientist at KCAS Bio is the role for you. 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. Depending on your background and qualifications, we may consider hiring you for one of three levels of Scientist roles at KCAS Bio. This will be determined during the interview process. (Please note this is a representative summary of responsibilities, not a comprehensive or exclusive list of the duties to be performed in any position. Employees must follow instructions and perform additional duties as requested.) WHO YOU ARE You will thrive at KCAS Bio if you enjoy a relational environment, are purpose- and values-driven, embrace constant development and supportive leadership, and enjoy being part of innovative work. WHAT YOU’LL GET Our benefits include, and extend beyond, the traditional package. At KCAS Bio, you will enjoy company sponsored events like food trucks, family days and spirit days. You will grow in your career with KCAS University. You will be able to connect with like-minded employees to further KCAS Bio's approach to key areas such as wellness, inclusion, and community outreach. You will engage as an owner in our stock ownership program. You will have access to the latest technology. And you will be able to invest in the community with paid time off to volunteer. Learn more about the Benefits at KCAS Bio WHO WE ARE We are a fast-growing contract research organization (CRO) headquartered in Kansas City, pioneering the latest drug development in both human and animal health fields. Demand for our expertise is growing and so is our need for great people to work in nimble, empowered teams committed to one another’s growth. At KCAS Bio, we advance both great science AND great people. Learn more about what it is like to work at KCAS Bio KCAS Bio is proud to be an Equal Opportunity Employer. Among other things, we provide equal employment opportunities without regard to race, color, religion, national origin, ancestry, marital status, veteran status, age, disability, pregnancy, genetic information, sex, sexual orientation, gender identity, or any other legally protected category; we recruit qualified candidates without regard to citizenship status based on internal processes that enable us to hire the right candidates consistent with the appropriate U.S. Immigration framework; and (3) we work with and provide reasonable accommodations to individuals with disabilities and for sincerely held religious beliefs, observances, and practices. Anyone who needs reasonable accommodation may send an email to [email protected] or call 913-248-3000 (for TTY assistance call 711) and ask for Human Resources. IND123 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

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