Universal Diagnostics S.L. (UDX) is a Spanish in-vitro diagnostics company developing a platform of minimally-invasive, blood-based solutions for detecting cancer early when treatment options are more plentiful and survival rates are still high. Backed by MedTech Innovator.
About the role
We are seeking a highly motivated Research Scientist II specializing in Reagent QC Development to join our rapidly growing team. This role will play a critical role in developing and executing quality control (QC) methods for reagents used in our NGS-based diagnostic assays.
What they're looking for
- Master’s degree or Ph.D. in Molecular Biology, Biochemistry, Genetics, or a related field
- 3 + years of experience in development reagent QC methods for NGS-based IVD assays
- Understanding of reagent QC method development, including functional and stability testing
- Familiarity with regulatory requirements (e.g., FDA, IVDR) and industry standards (e.g., CLSI guidelines)
- Proven ability to design and manage validation studies
- Excellent analytical, problem-solving, and project management skills
More about this role
Universal D X , Inc . is an international Company with a highly experienced team focused on cracking cancer’s code. Through our multi-omics and bioinformatics models, we have figured out how to read the disease’s signals in blood with high accuracy to detect cancer in its earliest stages. Starting with a colorectal cancer screening liquid biopsy test , we are building a multi-cancer platform that can identify the unique DNA regions associated with different types of cancers.
We are seeking a highly motivated Research Scientist II specializing in Reagent QC Development to join our rapidly growing team. This role will play a critical role in developing and executing quality control (QC) methods for reagents used in our NGS-based diagnostic assays. Reporting to the Director, Reagent Development, this role will oversee reagent QC method development as well as establish reagent freeze/thaw (F/T) stability and onboard reagent stability to ensure robust assay performance and compliance with regulatory standards. This role will also play an integral role in coordinating the transfer of reagent QC methods and related documentation to the Reagent Manufacturing team.
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