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Open nowPosted 6 days agoWe saw it 48 min after it went up

Principal Program Manager

Universal DX9 open roles

Where
United States
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Your applicationOpen nowPrincipal Program ManagerUniversal DX · United States

  1. YouYes, apply to this one.

  2. CV RocketCV written for this posting.

  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

  4. CV RocketApplied on Universal DX's own form.

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The clock on this job

Early applications get read.

8.0% of postings close within 7 days. Measured by our own scanner across the market. Universal DX postings stay open a median of 9 days.

Share of postings closed within
  1. 1.6%1 day
  2. 3.5%3 days
  3. 8.0%7 days
  4. 14.9%14 days
  5. 34.1%30 days
This job: posted 6 days ago

Universal DX median: 9 days open

The posting

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:

Universal DX is seeking a highly experienced program manager to join our growing Program Management team. Reporting to the Director, Program Management, this role will partner closely with Assay Development, Reagent Development, and Pre-Analytical Development to translate scientific and product strategy into executable plans. The role will serve as the primary program-management bridge between wet-lab Product Development and Automation, Software Development, Quality, Regulatory, Lab Operations, Manufacturing, Supply Chain, and other cross-functional partners supporting development and commercialization of Universal DX IVD products.

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:

  • Lead integrated planning and support execution for assay, reagent, and pre-analytical development workstreams across the IVD product lifecycle.
  • Partner with scientific and functional leads to define scope, deliverables, success criteria, resources, budgets, timelines, and decision points.
  • Connect wet-lab plans with automation and software development, ensuring requirements, interfaces, dependencies, and verification activities remain aligned.
  • Coordinate with Quality, Regulatory, Lab Operations, Clinical, Manufacturing, and Supply Chain so design-control and operational deliverables are incorporated into the program plan.
  • Proactively identify planning gaps, technical and execution risks, and change impacts; develop options and mitigation plans and escalate with clear recommendations.
  • Facilitate cross-functional working sessions and workstream meetings; document decisions, actions, owners, and due dates and drive timely closure.
  • Maintain integrated schedules, dashboards, and executive-ready reporting, while mentoring PM colleagues and strengthening consistent planning practices across Product Development.

What you'll bring:

  • Bachelor's degree in biology, chemistry, biotechnology, bioengineering, or a related scientific or engineering discipline; an advanced degree is preferred.
  • Eight or more years of relevant experience in diagnostics, medical devices, or life science product development, including substantial responsibility for complex cross-functional programs.
  • Direct IVD product development experience gained either as a scientist or technical lead who has driven program execution, or as a program manager dedicated to Product Development functions.
  • Demonstrated experience supporting wet-lab product development functional areas and working cross-functionally with other functions.
  • Strong working knowledge of regulated product development, design controls, risk management, verification and validation, and design history file deliverables under an ISO 13485 quality system.
  • Ability to understand scientific and technical content, ask effective questions, research alternatives, and translate complex work into clear plans and decisions.
  • Strong facilitation, stakeholder management, written communication, and executive presentation skills, with the ability to influence without direct authority.
  • Proficiency with program management methods and tools; experience with Smartsheet, Jira, Confluence, and Microsoft 365 and a PMP or similar certification are highly preferred.

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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