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 Senior Manufacturing Engineer to coordinate cGMP manufacturing, stability program execution within Manufacturing Operations. This onsite role will provide technical and operational oversight for schedules, sample pulls, testing readiness, traceability, records, and cross-functional follow-up while partnering closely with the FQC Technical Lead and Quality.
What they're looking for
- Coordinate cGMP manufacturing and stability programs
- Develop and maintain FQC and stability schedules, including sample-pull and testing timelines
- Coordinate stability sample storage, inventory, pulls, testing, and associated documentation
- Ensure stability activities are executed according to approved protocols and defined time points
- Maintain stability study records, trackers, sample inventories, and traceability
- Monitor FQC and stability data for trends, unexpected results, and operational concerns
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 Senior Manufacturing Engineer to coordinate cGMP manufacturing, stability program execution within Manufacturing Operations. This onsite role will provide technical and operational oversight for schedules, sample pulls, testing readiness, traceability, records, and cross-functional follow-up while partnering closely with the FQC Technical Lead and Quality. The ideal candidate is organized, technically strong, comfortable with regulated laboratory workflows, and able to translate approved protocols into reliable day-to-day execution.
You will be part of a team that is passionate about developing novel diagnostic tests for the early detection of cancers. As part of the team, you will be in a...
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