Assay Development Scientist, Genomics Services

Assay Development Scientist, Genomics Services Are you a dedicated scientist with expertise in molecular genetics and genomics technology? Join CellCarta's Genomics Services team as an Assay Development Scientist and contribute to the development, validation, and implementation of cutting-edge qPCR, dPCR, and NGS assays for clinical trials. In this role, you will manage and execute technical laboratory studies, troubleshoot data, and collaborate with cross-functional teams to ensure the successful and timely delivery of projects meeting regulatory standards. Your strong foundation in molecular genetics, along with your experience in NGS, will be invaluable in this role. If you're a self-motivated, detail-oriented scientist with a passion for innovation and problem-solving, we invite you to join our dynamic team in Naperville, Illinois. Summary As an Assay Development Scientist within our Genomics Services team, you will be responsible for the implementation, development, and validation of high-quality qPCR, dPCR, and NGS assays for use in clinical trials, utilizing state-of-the-art RNA and DNA technologies. Responsibilities More specifically, you will: Manage, plan, create, and execute complex technical and laboratory studies for small teams, including writing protocols and reviewing and approving documents within design control procedures Conduct laboratory procedures to support the development or implementation of assays across different workflows Troubleshoot and perform technical interpretation of data; evaluate and document studies; analyze and present results in written reports Work collaboratively with team members and colleagues from other functions to ensure projects are delivered safely, effectively, and efficiently to the required quality and regulatory standards in a timely manner Develop and present data for internal and external projects Prepare for and lead departmental and client meetings Education Master's or PhD in Life Sciences (preferably Biology, Biomedical Sciences, Bioengineering, Pharmaceutical Sciences, or Biochemistry) Qualifications & Requirements Minimum of 3 years of relevant professional experience in a highly regulated environment Solid foundation in molecular genetics and genomics technologies is essential Experience with assay development using qPCR, dPCR, or NGS is required Experience with NGS troubleshooting is required Experience working in a regulated environment (ISO 13485) is a plus Strong computer skills and significant experience with Microsoft Excel, PowerPoint, and Word are required Demonstrated excellent problem-solving and decision-making abilities Results-oriented, creative, and analytical thinker with a proactive mindset Proven organizational skills, self-motivation, accountability, and attention to detail Ability to manage and prioritize multiple projects effectively Strong troubleshooting, data analysis, and interpretation skills Flexible, sociable, diplomatic, a team player, inspirational, and a strong communicator Eager to learn and assimilate new concepts Working Conditions Full-time permanent position, 100% onsite, Monday through Friday Benefits We offer a wide range of benefits including: Competitive wages: $69,800-$93,000 USD Medical, dental, and vision benefits 401(k) retirement savings plan with a healthy match Vacation and sick time Career development opportunities About CellCarta CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics, and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The Company operates globally with facilities located in Canada, USA, Belgium, Australia, and China. Joining CellCarta means working with dedicated professionals who are focused on achieving our mission of impacting the future of patient therapy. We make a difference in the lives of patients around the world! Join us as we make an impact on patient therapy! The information collected to review your application will be processed by the human resources services of CellCarta Biosciences Inc. and its affiliates (collectively, "CellCarta"). The legal basis for this processing is the legitimate interest of CellCarta to evaluate the suitability of candidates for the roles available at CellCarta. CellCarta will only process that information which is necessary to evaluate your application. This information includes identifying information such as your name, address, email address and phone number, as well as information about your education and professional experience, including previous positions and your CV. Such information is required for us to complete your applicant file, assess your suitability for the role and comply with applicable laws. CellCarta may obtain personal information from other sources, such as during reference, background, or employment checks, with your permission, and from third party sources such as recruitment and assessment sites or professional social media sites, in each case only if such information is relevant to reviewing your application. Your personal information will be retained only for so long as reasonably necessary and in accordance with applicable laws. This information will be processed confidentially and only accessed by those who have a need for the recruitment process. Please note that the information comprising your applicant file may be processed in a country that is not where you are located (for example, you might be in the European Economic Area or Québec, Canada, whereas your applicant file may be reviewed by CellCarta in the United States). If you are offered and accept employment with CellCarta Biosciences Inc. or one of its affiliates, the information collected will become part of your employment record. If you do not want us to retain your information, or want us to update it, please contact privacy@cellcarta.com .