Midjourney
Midjourney is a non-profit research lab that is investigating new thought mediums to improve the human species' inventive abilities.
- Open roles
- 20
- New role every
- ~3.9 days
Company signals
Score: 86Job facts
- Location
- Remote · United States of America
- Also in
- Anywhere
- Workplace
- Remote
- Type
- Full-time
- Department
- Midjourney Medical
- Posted
- Jun 30, 2026
Last verified live 10 hours, 6 minutes ago · checked directly on the company's Ashby
More roles at Midjourney
- Principal Electrical Engineer (Design Lead) · San Francisco
- QA Analyst · SF or NY Hybrid
- Product Manager · San Francisco Bay Area Hybrid
- Engineering Manager · San Francisco Bay Area Hybrid
- Backend Engineer, Core Systems · San Francisco Bay Area Hybrid
- Backend Engineer, Product · San Francisco Bay Area Hybrid
Quality Director (Medical Device / USCT)
at Midjourney
What you’ll do
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Own and evolve the Quality Management System (QMS) to support a regulated medical device development program, including design controls and DHF maintenance.
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Establish and enforce requirements traceability: user needs → design requirements → verification/validation artifacts and change control.
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Define and run the program-level V&V strategy (verification, validation, and test coverage), including test plans, protocols, reports, and acceptance criteria.
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Drive risk management activities (e.g., DFMEA / PFMEA, hazard analyses) and ensure mitigations are reflected in requirements and verification.
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Lead document control: reviews, approvals, training, retention, and audit readiness.
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Partner with engineering to make quality “native” to the dev workflow (automated testing, release gates, software configuration management).
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Prepare the program for audits and inspections, including hands-on audit leadership.
What we’re looking for
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Senior experience leading quality for complex hardware + software products in a regulated environment.
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Deep familiarity with design controls, DHF, document control, risk management, and verification planning.
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Strong systems thinking and the ability to translate ambiguous product intent into testable requirements.
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Comfortable collaborating directly with multidisciplinary engineering (recon/ML, embedded, mechanical, EE, cloud).
Useful experience
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Regulated product quality leadership (ISO 13485 / 21 CFR 820 or equivalent), including audit readiness and FDA-facing work.
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eQMS + document control fluency (e.g., Greenlight Guru) that integrates cleanly with modern engineering workflows.