The Role
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.
Summary Generated by Built In
Performing critical work that impacts our industry and our world’s health while problem solving and innovating in the field – that is what Associate Scientists at KCAS Bio get to do every day. If that gets you excited too, then maybe working as an Associate Scientist at KCAS Bio is the role for you.
When you work as an Associate Scientist on the BioPharma Molecular team at KCAS, you get to further our mission by applying your knowledge of molecular and cell biology techniques to support the design, development, validation, and analysis of bioanalytical methods and samples. You will work with technologies such as qPCR and ddPCR and support cell-based assays within a GLP (Good Laboratory Practice) regulated laboratory environment.
Our BioPharma Molecular team provides a full range of molecular services and viral vector capabilities to support gene replacement, gene addition, gene inhibition, gene editing, and cell therapy or transplantation programs throughout drug development.In this role, we will rely on you to:
- Demonstrate technical and scientific skills in molecular technologies, including PCR (qPCR and ddPCR) and the handling of DNA and RNA
- Perform extraction and quantification of nucleic acids from a variety of biological matrices
- Work with human blood, primary cells and tissues, and perform associated cell culture activities at the BSL-II level
- Plan and carry out assigned experiments, including method development, method validation, sample analysis, data calculation, interpretation, review, and troubleshooting
- Support the design of experiments and evaluate outcomes against current SOPs, protocols, and other applicable standards, recommending appropriate courses of action as needed
- Analyze and interpret scientific data, prepare summary tables, and review raw data for accuracy, completeness, and integrity
- Assist with the preparation and review of SOPs, study plans, and reports
- Maintain materials, equipment, and instrumentation required to support successful study execution
- Provide work instructions and technical training to more junior scientific staff as appropriate
- Maintain accurate and complete documentation in compliance with study protocols, SOPs, Good Documentation Practices (GDP), and GLP regulatory requirements
- Troubleshoot technical issues, identify potential causes, and escalate complex challenges appropriately
- Manage multiple assignments and priorities while meeting established study timelines and deadlines
- 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 Microbiology, Biochemistry, Chemistry, Immunology, Molecular Biology, or related scientific field with at least 4 years of experience in a scientific laboratory environment
- Hands-on experience working in a GLP-regulated laboratory environment and strong knowledge of Good Documentation Practices (GDP)
- Experience with molecular technologies, including PCR, qPCR, and/or ddPCR
- Experience handling DNA and RNA, including nucleic acid extraction and quantification
- Experience working with human blood, primary cells and/or tissues in a BSL-II laboratory environment
- Experience with assay design, method development, validation, and sample analysis
- Experience analyzing and interpreting data, preparing summary tables, and reviewing raw data
- Ability to troubleshoot technical and scientific challenges using sound critical-thinking and problem-solving skills
- Ability to manage multiple priorities and meet established deadlines
- Excellent verbal and written communication and organizational skills
- Self-motivated, flexible, and adaptable, with the ability to work independently and collaboratively within a team environment
(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
Skills Required
- Bachelor's, master's, or PhD in Microbiology, Biochemistry, Chemistry, Immunology, Molecular Biology, or a related scientific field
- At least 4 years of experience in a scientific laboratory environment
- Hands-on experience in a GLP-regulated laboratory environment
- Strong knowledge of Good Documentation Practices
- Experience with PCR, qPCR, and/or ddPCR
- Experience handling DNA and RNA, including nucleic acid extraction and quantification
- Experience working with human blood, primary cells, and/or tissues in a BSL-II laboratory environment
- Experience with assay design, method development, validation, and sample analysis
- Experience analyzing and interpreting data, preparing summary tables, and reviewing raw data
- Ability to troubleshoot technical and scientific challenges using critical-thinking and problem-solving skills
- Ability to manage multiple priorities and meet established deadlines
- Excellent verbal and written communication and organizational skills
- Self-motivated, flexible, adaptable, and able to work independently and collaboratively
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The Company
What We Do
With its presence in three locations across North America and Europe, KCAS Bio is a leading contract research organization (CRO) employing top scientific talent and providing comprehensive bioanalytical services to the global biopharmaceutical industry from early discovery support through product registration and beyond. The collaboration of the three entities allows for global support in bioanalytical, biomarker, immunogenicity, cellular and molecular assay services along with clinical kitting and sample management. The KCAS family of companies operates in state-of-the-art facilities in the United States and Europe. This business structure enables the expertise, capacity, and flexibility to support the development of all types of drugs, biologics, cell and gene therapies to improve health worldwide. Our purpose is to help accelerate the discovery and development of life-changing drugs smoothly, safely and sustainably.
