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Home›Jobs›Tempus›Lab Manager, Molecular Operations
Tempus

About Tempus

Transforming healthcare with data-driven insights

🏢 Tech👥 1K-5K📅 Founded 2015📍 Chicago, Illinois, United States

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...

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Tempus

Lab Manager, Molecular Operations

Tempus • Durham, NC

Posted 8 months ago🏛️ On-SiteMid-LevelLaboratory manager📍 Durham
Apply Now →

Job Description

With the advent of genomic sequencing, we can finally decode and process our genetic makeup. We now have more data than ever before but providers don't have the infrastructure or expertise to make sense of said data. Here at Tempus, we believe the greatest promise for the detection and treatment of cancer lies in the deep understanding of molecular activity for disease initiation, progression, and efficacious treatment based on the discovery of unique biomarkers.

We're on a mission to connect an entire ecosystem to redefine how genomic data is used in clinical settings. We are looking for a Manager to join a laboratory operations team who are passionate and focused on developing state of the art techniques for processing and creating and interpreting vast amounts of genomic and molecular data. You will collaborate with technology, research, and business development teams to develop the most advanced sequencing platform in cancer care.

Shift - Tuesday-Saturday (11:00am-7:30pm)

What you’ll do:

Laboratory Oversight & Performance Metrics

  • Provide high-level oversight of lab operations, ensuring efficient execution of daily workflows while maintaining compliance with CAP, CLIA, and OSHA standards.
  • Deliver regular updates to upper management , summarizing laboratory performance, turnaround times, instrument downtime, productivity, and project progress.
  • Lead initiatives to enhance data tracking and reporting on lab metrics, identifying trends and areas for improvement.

Process Management

  • Oversee and drive multiple continuous improvement initiatives, change orders, and assay implementations from inception to completion.
  • Develop and maintain project timelines, ensuring alignment with laboratory goals, CAP/CLIA regulatory requirements, and resource constraints.
  • Identify bottlenecks in workflow efficiency and implement process optimizations to enhance turnaround time and lab performance.
  • Partner with cross-functional teams, including R&D, quality assurance, and regulatory teams, to ensure seamless project execution and regulatory compliance.
  • Monitor key project milestones, anticipate risks, and proactively address issues to prevent delays or deviations.

Technical Leadership & Team Development

  • Serve as a key liaison between laboratory teams and project stakeholders, translating technical and operational needs into actionable project plans.
  • Mentor and guide laboratory staff, ensuring ongoing professional development and competency in NGS workflows.
  • Collaborate with leadership to develop strategies for resource allocation, process automation, and lab efficiency enhancements.

Regulatory & Quality Compliance

  • Ensure all process improvements, new assay implementations, and workflow modifications meet CAP/CLIA standards.
  • Maintain and update standard operating procedures (SOPs) to align with evolving best practices and regulatory expectations.
  • Oversee QC reviews, ensuring data integrity and validity, and implement corrective actions when test systems deviate from expected performance.

Preferred Qualifications:

  • One of the following educational requirements:
    • M.S. (physical, chemical, or biological science) + at least 4 years pertinent clinical lab experience (at least 2 of which are in a high-complexity molecular laboratory)
    • BS in clinical laboratory science, chemical, physical or biological sciences and at least 7 years of pertinent clinical lab experience in a high-complexity molecular laboratory
  • Demonstrated experience leading assay development and process improvement projects 
  • Strong background in Next-Generation Sequencing (NGS) and molecular diagnostics.
  • Proven track record of successfully managing multiple projects, ensuring timely completion and regulatory compliance.
  • Strong organizational skills and project management experience (i.e. familiar with gantt charts and other organizational tools)
  • Strong leadership abilities, with a high degree of personal and professional integrity.
  • Excellent communication and collaboration skills, with experience working cross-functionally across departments.
  • Ability to adapt to a fast-paced, evolving environment and drive strategic improvements.
  • Experience with Lean Six Sigma methodologies, process optimization, and/or laboratory automation is a plus.
#LI-SH1
#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.

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