
About Tempus
Transforming healthcare with data-driven insights
Key Highlights
- Largest library of clinical and molecular data in the world
- Headquartered in Chicago, Illinois
- Over $1 billion raised from top-tier investors
- 1,000+ employees dedicated to healthcare technology
Tempus, headquartered in Chicago, Illinois, is a technology company that has developed the largest library of clinical and molecular data, focusing on oncology. With over 1,000 employees, Tempus partners with leading healthcare institutions to provide data-driven insights and personalized treatment ...
🎁 Benefits
Tempus offers competitive salaries, equity options, generous PTO, flexible remote work policies, and comprehensive health benefits, including parental...
🌟 Culture
Tempus fosters a culture of innovation and collaboration, emphasizing data-driven decision-making and a commitment to improving patient outcomes throu...
Overview
Tempus is hiring a Principal Quality Engineer to lead quality assurance for their In Vitro Diagnostics and Laboratory Developed Test products. You'll apply your expertise in product development and risk management to ensure the highest quality standards. This role requires significant experience in quality principles and practices.
Job Description
Who you are
You have extensive experience in quality engineering, particularly within the healthcare or medical device sectors. Your background includes a deep understanding of quality assurance principles and practices, especially as they relate to regulated products. You are skilled in risk management and have a proven track record of implementing quality systems that ensure compliance and continuous improvement.
You thrive in multidisciplinary teams and enjoy collaborating with subject-matter experts to drive product quality throughout the lifecycle. Your analytical skills allow you to effectively review data for product verification and validation, ensuring that all products meet the necessary standards before reaching the market.
What you'll do
As the Principal Quality Engineer at Tempus, you will be responsible for implementing quality assurance principles and practices for the design and maintenance of assay products and manufacturing processes. You will lead product risk management activities during initial product realization and throughout product changes, both pre- and post-launch. Your role will involve analyzing and reviewing data to ensure the relevance, adequacy, and effectiveness of Tempus' Quality Management System (QMS).
You will maintain and execute the change management process, ensuring that all changes are assessed for impact and that appropriate action items are addressed. Your proactive and preventive risk-based approach will be crucial in driving continuous improvement within the organization. You will also be responsible for ensuring compliance with legal and ethical standards regarding intellectual property and protected health information.
What we offer
At Tempus, you will be part of a mission-driven organization that is at the forefront of precision medicine. We offer a collaborative work environment where your contributions will directly impact the healthcare industry. You will have the opportunity to work with cutting-edge technology and be part of a team that is dedicated to improving patient outcomes through innovative solutions. We encourage you to apply even if your experience doesn't match every requirement, as we value diverse perspectives and backgrounds.
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