Quality Engineer

Posted 10 Days Ago
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Chicago, IL
Hybrid
Junior
Artificial Intelligence • Big Data • Healthtech • Machine Learning • Analytics • Biotech
Tempus is a data-driven precision medicine company bringing the power of data and artificial intelligence to healthcare.
The Role
The Quality Engineer will implement quality assurance principles for the design and maintenance of medical devices and tests. Responsibilities include risk management, quality document review, audits, root cause investigations, process validation, and monitoring of quality metrics. This role demands collaboration in a fast-paced project environment.
Summary Generated by Built In

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.

The Quality Engineer will work in a multidisciplinary team of subject-matter-experts in the development and sustaining of Tempus’ In Vitro Diagnostics (IVD) medical devices and Laboratory Developed Test (LDT) products. This is a hands-on role where the Quality Engineer will apply diversified knowledge in the areas of product development, risk management and quality principles and practices throughout the entire lifecycle of Tempus’ regulated products.

Responsibilities include the following:

  • Responsible for implementation of quality assurance principles and practices for design and maintenance of Tempus’ assay products and manufacturing processes
  • Responsible for product risk management activities during initial product realization and during product changes, pre- and post-launch
  • Responsible for quality assurance review for correctness and completeness of Tempus documents and records
  • Participate in the planning and development of project DHF and DMR documentation
  • Participate in internal and external quality system audits as required
  • Participate in root cause investigations as quality events/incidents arise
  • Participate in design transfer and process validation activities
  • Coordinate identification and monitoring of quality metrics and indicators
  • Coordinate change management process, ensuring change impact and action items are appropriately evaluated, tested and documented
  • Support other duties as assigned

Qualifications 

  • 2+ years of experience in the Medical Device/Pharmaceutical regulated industry.
  • BS degree in Engineering field such as Biomedical, Bioengineering or Chemical Engineering
  • Experience with applicable FDA, European and other relevant clinical/regulatory requirements, international standards, including ISO 9001, ISO 13485, ISO 14971, EU IVDR/MDR and 21 CFR 820, etc.
  • Experience working in a fast-paced project core-team environment
  • Excellent oral and written communication skills and can communicate at multiple levels in the organization
  • Proficient in Microsoft Office (Word, PowerPoint, Excel, etc.)
  • Proficient in eQMS systems (Jama, ETQ, Pilgrim SmartSolve, etc.)
  • Analytical skills and ability to understand technical data
  • This position is onsite





#LI-SH1#LI-Hybrid#LI-Onsite

We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.


Additionally, for remote roles open to individuals in unincorporated Los Angeles – including remote roles- Tempus reasonably believes that criminal history may have a direct, adverse and negative relationship on the following job duties, potentially resulting in the withdrawal of the conditional offer of employment: engaging positively with customers and other employees; accessing confidential information, including intellectual property, trade secrets, and protected health information; and appropriately handling such information in accordance with legal and ethical standards. Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law, including the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.

Top Skills

Eu Ivdr
Eu Mdr
Fda
Iso 13485
Iso 14971
Iso 9001

What the Team is Saying

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The Company
HQ: Chicago, IL
2,482 Employees
Hybrid Workplace
Year Founded: 2015

What We Do

Tempus is a technology company advancing precision medicine through the practical application of artificial intelligence in healthcare. With one of the world’s largest libraries of clinical and molecular data, and an operating system to make that data accessible and useful, Tempus enables physicians to make near real-time, data-driven decisions to deliver personalized patient care and in parallel facilitates discovery, development and delivery of optimal therapeutics.

The goal is for each patient to benefit from the treatment of others who came before by providing physicians with tools that learn as the company gathers more data. For more information, visit tempus.com.

Why Work With Us

We're looking for those who challenge the status quo. For the builders who are never done building and the learners who are never done learning. We're looking for unwavering commitment and undying curiosity. We're looking for the smartest people on the planet to attack one of the most challenging problems mankind has ever faced.

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Tempus AI Offices

Hybrid Workspace

Employees engage in a combination of remote and on-site work.

Most of the team follows a hybrid policy, with some roles allowing for a fully remote arrangement and some roles being onsite only.

Typical time on-site: 3 days a week
Company Office Image
HQChicago, IL
Boston, MA
New York, NY
Peachtree Corners, GA
Raleigh, NC
Redwood, CA
Learn more

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