Tempus

NGS Senior Scientist 1

Tempus$95K — $120K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Ph.D. in molecular biology or related field, or Master's with 5+ years of experience.
  • Experience in assay development and validation is a must.
  • Clinical laboratory experience is required; familiarity with CAP/CLIA/NYSDOH is preferred.
  • Strong analytical, troubleshooting, and experimental design capabilities.
  • Detail-oriented and highly organized with a commitment to quality.
  • Ability to learn quickly and adapt to new technologies and workflows.
  • Proven collaboration skills across teams and excellent communication skills.
  • Capability to manage multiple priorities in a fast-paced setting.

Responsibilities

  • Lead development of molecular assays and NGS workflows for high-throughput laboratories.
  • Design, execute, and analyze R&D studies with scientific rigor.
  • Validate assays and support clinical implementation from design to launch.
  • Execute qualification studies for reagents and methods for clinical deployment.
  • Troubleshoot issues in data interpretation and drive process improvements.
  • Collaborate with cross-functional teams, providing scientific leadership.
  • Train and mentor junior staff on new laboratory workflows.
  • Support automation initiatives to enhance laboratory efficiency.
  • Adapt quickly to changing priorities in a dynamic work environment.

Benefits

  • Incentive compensation options available.
  • Restricted stock units offered.
  • Comprehensive medical benefits.
  • Additional benefits based on position.
  • Support for professional development and continued education.
Full Job Description
We are seeking a Senior Scientist to lead the development and validation of new molecular assays and laboratory processes for deployment in our clinical laboratory.

What You'll Do
  • Lead development of molecular assays and NGS workflows for high-throughput clinical laboratories.
  • Design, execute, and analyze R&D studies with scientific rigor and attention to detail.
  • Lead assay validation and clinical implementation from study design through launch, including workflow development, SOP creation, and documentation.
  • Design and execute qualification and validation studies for reagents, instruments, equipment, and methods to support clinical deployment.
  • Interpret data, troubleshoot issues, and drive process improvements.
  • Collaborate across cross-functional teams and provide scientific leadership in a matrixed environment.
  • Communicate clearly and effectively with technical and non-technical stakeholders.
  • Train and mentor junior scientific staff and support implementation of new laboratory workflows.
  • Support automation and technology initiatives to improve laboratory workflows.
  • Manage multiple priorities and adapt quickly in a fast-paced environment.
  • Travel up to 10% as needed.

Qualifications
  • Ph.D. with 0 or more years of experience, or Master's degree with 5+ years of relevant experience in molecular biology, assay development, or a related field.
  • Experience in assay development and/or validation required.
  • Experience in a clinical laboratory environment required; CAP/CLIA/NYSDOH experience preferred.
  • Strong analytical, troubleshooting, and experimental design skills.
  • Highly organized, detail-oriented, and committed to quality and accuracy.
  • Proven ability to learn quickly and adapt to new processes, technologies, and workflows.
  • Strong collaboration skills with the ability to lead across teams.
  • Excellent oral and written communication skills.
  • Ability to manage competing priorities and deadlines in a dynamic environment.

Preferred Technical Experience
  • DNA/RNA extraction and purification methods.
  • NGS library preparation, hybrid capture, and sequencing workflows.
  • PCR-based techniques, including PCR, qPCR, RT-PCR, and ddPCR.
  • Nucleic acid manipulation, quantitation, and analysis.
  • Assay troubleshooting, root cause analysis, and workflow optimization.

Highly Desirable
  • Experience with FFPE tissue workflows.
  • Experience with laboratory automation and liquid handling robotics.
  • Experience developing and implementing protocols for CLIA-regulated laboratories.
  • Familiarity with LIMS and laboratory data systems.


Pay Range: $95,000 - $120,000 USD

The expected salary range may vary for other locations. Actual salary may vary based on qualifications and experience. Tempus offers a full range of benefits, which may include incentive compensation, restricted stock units, medical and other benefits depending on the position.

About Tempus

Tempus is a technology company that has built an operating system to battle cancer. The company enables physicians to deliver personalized cancer care for patients through its interactive analytical and machine learning platform. Tempus provides genomic sequencing services and analyzes molecular and therapeutic data to empower physicians to make real-time, data-driven decisions. The company also offers research services to enable discovery of new therapeutic targets and clinical services that support clinical trial design and monitoring. Tempus was founded in 2015 by Eric Lefkofsky and has raised over $8 billion in funding to date.
Learn more about Tempus
Size
1,001 employees
Industry
Founded
2015

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