Quality Assurance (QA) Specialist

Tempus AIChicago, IL
$55,000 - $70,000Onsite

About The Position

Passionate about precision medicine and advancing the healthcare industry? Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.

Requirements

  • Superb organizational and follow through skills
  • Willingness to learn applicable quality standards, regulations, and internal procedures.
  • Strong interpersonal skills in the areas of written and verbal communication
  • Must be creative, flexible, and able to prioritize and handle multiple projects concurrently
  • Must be self-motivated and have the ability to work with minimal supervision
  • Minimum of 1 year of QMS experience in the FDA regulated industry - medical devices or IVDs
  • Bachelor’s degree required preferably in a life science discipline
  • Exposure to internal audits, external audits, and inspections

Nice To Haves

  • Some QA experience in a molecular testing laboratory (LDTs) is a plus
  • Interest in obtaining Auditor certification is a plus

Responsibilities

  • Support Lead Auditor with audit functions
  • Participate in conducting internal audits under the direction of the Lead Auditor
  • Assist with completion of partnership pre-audit questionnaires
  • Oversee drafting of internal and external audit responses to closure
  • Administrative audit functions as needed
  • Lead partnership/client audits.
  • Communicate with partners as needed
  • Assist with client pre-qualification questionnaires regarding quality assurance (QA) and the quality management system (QMS).
  • Communication with Tempus’ Notified Body as needed
  • Comply with documented Quality Management System procedures
  • Completion of assigned training on time
  • Review QMS documentation against applicable regulations for international compliance
  • Remain up to date with applicable regulations to communicate changing requirements to Management
  • Track corrective and preventive actions (CAPAs), deviations, and follow-up activities related to audit outcomes
  • Assist with inspection readiness efforts and external audits
  • Help identify opportunities for process improvement related compliance and inspection readiness.
  • Managing and hosting external audits including regulatory inspections and CAP/CLIA Inspections.
  • Collaborate with cross-functional teams to collect documentation and support compliance activities.
  • Perform other duties and projects as assigned and ability to be flexible in supporting various quality system areas

Benefits

  • incentive compensation
  • restricted stock units
  • medical and other benefits depending on the position
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