A
bout
our Company:
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.
The Opportunity:
Universal DX is seeking a QA Specialist with strong expertise in document control and eQMS operations to join our growing Quality team. In this role, you will work closely with the QA Manager and other QA Specialists to ensure the accuracy, compliance, and continuous improvement of our global Quality Management System. You will play a key role in performing global document reviews, managing end?to?end eQMS processes, maintaining regulatory standards and requirements, overseeing training activities, and developing key quality metrics, between others. Your contribution will directly support the execution of our Quality strategy and enable the company's growth and expansion in the Life Sciences sector, particularly across the USA and the EU.
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 Company that aims more than to become one of the leaders in the industry. We want to have a huge positive impact on society by achieving the ambitious purpose of "making cancer a curable disease by detecting it earlier".
How you'll contribute:
Perform comprehensive integral document reviews to ensure accuracy, compliance, and alignment with applicable standards prior to formal approval.
Manage the end?to?end administration of the electronic Quality Management System (




eQMS
), ensuring data integrity, proper documentation lifecycle control, and
timely
execution of quality processes.
Coordinate document updates, revisions, and version control activities with global stakeholders to
maintain
consistency and regulatory compliance.
Monitor and
maintain
eQMS
workflows to support effective change control, training, and other quality?related processes.
Develop, track, and report key quality metrics to support performance monitoring and continuous improvement initiatives.
Conduct gap assessments to
identify
compliance risks, improvement opportunities, and alignment with internal and external quality and regulatory requirements.
Manage global standards and other regulatory or quality requirements to ensure the organization
maintains
up?to?date and compliant documentation.
Oversee training requirements within the
eQMS
, ensuring proper assignment,
timely
completion, and
accurate
training records.
Serve as
a central point
of contact for document control and
eQMS
?related queries, offering guidance and support to cross?functional teams.
What you'll bring:
Master's degree in Quality Management Systems.
Bachelor's degree.
Minimum 2 years of experience as quality consultant or quality specialist.
Good communication skills in English, both spoken and written.
Constancy, effort, patience and perseverance.
Be consistent, committed, competent, responsible and organized.
What we offer:
22 days of PTO.
PTO on your Birthday.
Flexible work schedule.
Remote work opportunities.
Flexible Remuneration with our partner Cobee.
Why Now?
This is an exciting time to be at Universal DX. We are growing rapidly and starting our US operations by building up our team, starting our lab and business operations, and establishing strategic partnerships.
We are looking for passionate changemakers to be a part of our journey in this expansive time for us.

📌 Qa Specialist (Málaga)
🏢 Universaldx
📍 Málaga