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À propos de ce poste Associate Manufacturing Engineer chez Universal DX

Universal DX · Sur site · Dallas Fort-Worth

About our Company: 

Universal DX, 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:

We are seeking an Associate Manufacturing Engineer to support hands-on Manufacturing and Functional QC activities for our diagnostic manufacturing operations. This onsite role is designed for a detail-oriented early-career professional who can execute routine laboratory and manufacturing tasks according to approved procedures, maintain accurate records, and support reliable day-to-day operational readiness. The ideal candidate is safety-conscious, organized, eager to learn, and comfortable working in a regulated environment where traceability and documentation quality are essential.

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”.

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.

Primary Focus:

Hands-on execution of routine Manufacturing and FQC activities in accordance with approved procedures.

How you’ll contribute:

  • Execute routine Manufacturing and FQC operations according to approved procedures and instructions.
  • Perform sample preparation, testing, reagent preparation, aliquoting, and other assigned operational activities.
  • Complete batch records, worksheets, and associated records accurately and contemporaneously.
  • Perform required equipment, workstation, and material setup activities.
  • Verify required materials, reagents, and consumables before beginning operations.
  • Maintain appropriate sample, material, reagent, and product identification and traceability.
  • Identify and promptly escalate deviations, unexpected results, documentation discrepancies, material issues, or equipment problems.
  • Support inventory management, operational readiness, and general Manufacturing activities as required.
  • Maintain required qualifications and cross-training across assigned Manufacturing and FQC processes.
  • Operate, clean, and maintain laboratory and manufacturing equipment in accordance with approved procedures and assigned schedules.
  • Follow biosafety, chemical safety, PPE, GDP, GMP, and QMS requirements at all times.
  • Communicate task status, delays, and issues clearly and contribute to a respectful, team-oriented work environment.

What you’ll bring:

  • Bachelor’s or Master’s degree in Bioengineering, Chemical Engineering, Molecular Biology, Biotechnology, Biochemistry, or a related field.
  • 0-3 years of experience in manufacturing, laboratory operations, QC, process engineering, or a related environment; relevant internship or academic laboratory experience may be considered.
  • Familiarity with basic laboratory techniques, pipetting/liquid handling, reagent preparation, sample handling, and controlled documentation practices.
  • Strong attention to detail and ability to follow written procedures, schedules, and instructions accurately.
  • Comfort working with laboratory/manufacturing equipment and maintaining clear identification and traceability of samples and materials.
  • Ability to recognize and promptly escalate deviations, unexpected results, documentation issues, and equipment/material concerns.
  • Reliable, organized, safety-conscious, and committed to continuous learning and cross-training.
  • Effective communication, teamwork, time-management, and basic problem-solving skills.

What we’ll offer:

We’re proud to offer exceptional corporate benefits which include:

  • 22 days of PTO with the possibility to carry over 10 days to the following year.
  • Company Holidays, plus your Birthday off!
  • Company-sponsored benefit plans, including medical, dental, and vision insurance plus life, STD, and LTD coverage, and 401(k).
  • Flexible work schedule.
  • And more to come!

 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. 

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