Associate Scientist – BioPharma LBA

Performing critical work that impacts our industry and our world’s health while problem solving and innovating in the field – that is what we get to do every day at KCAS Bio. If that gets you excited too, then maybe working at KCAS Bio is for you. When you work as an Associate Scientist in the BioPharma Sciences group at KCAS, you get to further our mission by learning and applying your knowledge in bioanalytical and scientific principles to support study execution and development activities under the guidance of senior scientists. You will begin building your foundation in assessing data integrity and troubleshooting with support. Our BioPharma Sciences team uses ligand binding assay (LBA) platforms to conduct bioanalytical testing in support of drug discovery, preclinical, and clinical studies, including the quantification of proteins, biomarkers, and anti-drug antibodies in biological matrices using technologies such as ELISA, MSD, and other immunoassay-based methods. (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'll rely on you to: Contribute to the planning of all phases of assigned projects including, R&D, ensure adequate supplies, method validation, test procedure preparation, sample analysis, data calculation, interpretation & review, troubleshooting and report preparation Design basic experiments & evaluate outcome vs. current SOPs, protocols other relevant standards with assistance; recommend appropriate course of action as necessary Be proficient in using common immunoassay platforms (ELISA, MSD, Luminex, etc) Provide work instructions and guidance to more junior scientific staff in the conducting of assigned projects Process and summarize data and interact with clients and/or auditors as necessary To qualify for this role, you will have: Bachelor of Science (BS) or Master’s degree in Chemistry, Immunology, Biochemistry, Biotechnology, Biology or related field, 2 years of experience in a regulated laboratory environment (GLP preferred) in large molecule immunoassay development/validation A minimum of 2 years working in an industry lab, CRO or Pharmaceutical setting (preferred) with GLP/GxP experience (a plus) Demonstrated lab experience utilizing biopharma analytical techniques (e.g. ligand binding assays including ELISA and ECL-based assays) Cell-based assays experience is a plus Maintain accurate experimental records in a GLP CFR21 Laboratory following SOPs Proficient at pipetting solutions and buffer preparation Skilled with Electronic Lab Notebook (ELN), Microsoft Excel, and Word to perform tasks

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