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GeneDx

Senior Quality Engineer

GeneDx · Remote

Posted about 2 months ago

or apply directly on GeneDx's site. We never take the application ourselves.

Is this posting real?

This role has been open
51 days
GeneDx's roles stay open a median of 67 days
Reposted
No
Salary listed
No
0% of GeneDx's roles list one
Ghost-job risk at GeneDx
high
30 stale, 0 reposted of 33 open
Hiring momentum
59 roles opened in the last 90 days
↑ up vs. the prior 90 days
Last confirmed on the employer's board
2026-10-24

Measured from postings appearing on and disappearing from GeneDx's own greenhouse board since 2026-08-03. Full hiring picture for GeneDx.

About this role

The Senior Quality Engineer at GeneDx will support the development and maintenance of quality management system (QMS) processes for IVD and software-enabled IVD products. This role involves executing QMS activities, drafting and maintaining quality documentation, serving as a quality representative on product teams, and facilitating risk management and compliance processes. The position also includes supporting audits and identifying process improvements while promoting a culture of quality and collaboration.

Our read on this posting2.8out of 5
benefits
1/5
freshness
4/5
career value
4/5
role clarity
5/5
pay transparency
0/5

Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of GeneDx as an employer.

What you need

  • Bachelor’s or advanced degree in a scientific, engineering, technical, or related discipline
  • Minimum of 6 years of Quality Engineering or Quality Assurance experience
  • At least 4 years of experience within an IVD, molecular diagnostics, or medical device regulated environment
  • Practical experience applying quality-system and product-development requirements in a regulated environment
  • Expertise in technical writing and QMS development
  • Strong understanding of the product development lifecycle

Nice to have

  • Experience using Ketryx or similar connected lifecycle management tools
  • Experience supporting regulatory submissions and audits/inspections
  • ASQ Certified Quality Auditor (CQA), ASQ Certified Quality Engineer (CQE), ISO 13485 Internal Auditor, and/or ISO 13485 Lead Auditor certification

Worth weighing

  • No specific mention of additional benefits or perks beyond competitive compensation
  • Fully remote position may require self-motivation and discipline
  • Standard work hours are Monday through Friday, 9 AM to 5 PM EST, which may not suit all candidates

Summarised from GeneDx's posting. Read the full original.

Listed by GeneDx on their greenhouse job board, last confirmed open on 2026-10-24. PitchMeAI is not the employer.

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