or apply directly on GeneDx's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 14 days GeneDx's roles stay open a median of 30 days
- Reposted
- No
- Salary listed
- No 0% of GeneDx's roles list one
- Ghost-job risk at GeneDx
- moderate 9 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
- 2026-09-17
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.
- 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 2026-09-17. PitchMeAI is not the employer.
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