Tempus AI

Tempus AI

Quality Assurance (QA) Specialist

Chicago · Mid

Sponsorship not specified$55k-$70kDetected 8 days ago
Process ImprovementPatient CareFDA RegulatoryMedical DevicesCommunication

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odds of building a lasting career here

36Risky
Cap-exempt (no lottery)0
Sponsors this role78
Entry-level history0
PERM / green-card track0
Lottery odds (Level I)39
Fits your clock70

Thin sponsorship signal and lottery-bound (~15% per draw). A low-probability bet with your clock running. Prioritize cap-exempt roles and proven entry-level sponsors first.

Lottery odds assume a STEM candidate.

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H-1B wage level

the lottery is wage-weighted — each level is one more entry

Level I · 1×
Level I$74,3811 entry
Level II$91,7492 entries
Level III$109,1383 entries
Level IV$126,5064 entries

The bottom of this range ($55,000) is below the Level I prevailing wage of $74,381. An H-1B cannot be filed below the prevailing wage, so an offer at the floor of this band could not be sponsored as posted.

DOL prevailing wage, 2026-27 wage year · Software Quality Assurance Analysts and Testers (15-1253) · Chicago-Naperville-Elgin, IL-IN. Wage level is derived by USCIS from the offered wage, occupation and worksite; the occupation shown is inferred from the job title.

Employer immigration record

from this employer's Department of Labor filings

Files H-1B transfers

6 transfer filings in the last year, covering 6 workers. Median labor-condition decision: 7 days. An employer that already files transfers is one that can take over an existing H-1B.

Sourced from Department of Labor LCA, PERM and prevailing-wage disclosure data. Employer matching is by name, so figures may be split across an employer's legal entities. Absence of a filing means none appears in our copy of the data, not that none exists.

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About the role

  • Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way.
  • CHI: $55,000-$70,000 The expected salary range may vary for other locations.

Responsibilities

  • Serve as a QA partner for assigned client-specific projects, coordinating quality activities, deliverables, timelines, risks, and follow-up actions.
  • Collaborate with project, product development, operations, regulatory, and other cross-functional teams to integrate quality requirements into project plans and execution.
  • Act as a professional, responsive point of contact for clients and external partners on assigned quality matters.
  • Support client onboarding, pre-qualification, and project-specific quality questionnaires
  • Manage and track NCRs, CAPAs, deviations, and related investigations, effectiveness checks, and follow-up activities associated with client projects.
  • Maintain awareness of applicable regulations and standards and communicate relevant changes or requirements to project stakeholders and management.
  • support response development and closure of project-related observations.
  • Perform other duties and projects as assigned, with flexibility to support additional quality system areas.
  • Support client onboarding, pre-qualification, and project-specific quality questionnaires; collect, review, and coordinate supporting documentation.
  • Participate in internal, external, client, and regulatory audits as a project quality representative; support response development and closure of project-related observations.

Requirements

  • Client-facing and audit-facing experience, with the ability to communicate quality requirements and project status clearly and professionally.

Skills

  • Strong written and verbal communication skills and the ability to work effectively with stakeholders at different levels.
  • Self-motivated, flexible, detail-oriented, and able to work with minimal supervision.
  • Willingness to learn and apply applicable quality standards, regulations, and internal procedures.
  • 1-3+ years of QA/QMS experience in a medical device, IVD, or other FDA-regulated environment.
  • Experience supporting internal audits, external audits, client audits, and/or regulatory inspections.
  • Experience in a molecular testing laboratory or with laboratory-developed tests (LDTs).
  • Familiarity with applicable FDA regulations and quality standards for medical devices and IVDs.
  • Preferred Experience
  • CHI: $55,000-$70,000
  • The expected salary range may vary for other locations.
  • Actual salary may vary based on qualifications and experience.

Compensation

  • The expected salary range may vary for other locations.

Benefits

  • Passionate about precision medicine and advancing the healthcare industry?
  • Perform other duties and projects as assigned and ability to be flexible in supporting various quality system areas

This listing is sourced directly from Tempus AI's careers page and normalized into a canonical job model.