Product · Full-time · San Francisco, United States
Company Overview
Headquartered in South San Francisco, CA, Cytovale is a dynamic, late-stage startup focused on developing a faster, more insightful way to diagnose fast-moving and immune-mediated diseases. Cytovale’s IntelliSep test is pioneering a new way of quickly and accurately analyzing white blood cells to stratify a patient’s risk of sepsis. The test simply and clearly determines risk of sepsis using a biomechanical evaluation of white blood cells collected from a standard blood draw, generating results in under 10 minutes. This gives physicians actionable information when they need it most, allowing them to confidently triage suspected sepsis patients quickly and spend more time with those in greatest need. It also helps strained health systems prevent unnecessary treatment, preserve valuable resources, and improve compliance with Sep-1 guidelines.
Job Description:
As a Quality Assurance Specialist, you will be responsible for supporting the product development life-cycle within the Cytovale QMS, and assist in the support of various quality system processes including Document Control, Receiving/Incoming Inspection/Release, Equipment Maintenance, Materials Control, CAPAs, Deviations, NCRs, Training, Labels, Internal Audits, etc.
Successful candidates will work well in a fast-paced startup environment, can balance priorities, demonstrate a hands-on and can-do attitude, embrace new challenges, enjoy collaborative efforts, peer coaching, and improving Quality System processes.
Primary Responsibilities:
Minimum Qualifications:
Preferred Qualifications:
Additional Details:
Cytovale has a mandatory COVID-19 vaccination policy.
This position will be based in the South San Francisco Bay area in an onsite work environment.
Ability to work in the United States.
Open roles at Cytovale