Senior Scientist Technical Operations 4375
Company: GRAIL Inc
Location: Durham
Posted on: January 12, 2026
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Job Description:
Our mission is to detect cancer early, when it can be cured. We
are working to change the trajectory of cancer mortality and bring
stakeholders together to adopt innovative, safe, and effective
technologies that can transform cancer care. We are a healthcare
company, pioneering new technologies to advance early cancer
detection. We have built a multi-disciplinary organization of
scientists, engineers, and physicians and we are using the power of
next-generation sequencing (NGS), population-scale clinical
studies, and state-of-the-art computer science and data science to
overcome one of medicine’s greatest challenges. GRAIL is
headquartered in the bay area of California, with locations in
Washington, D.C., North Carolina, and the United Kingdom. It is
supported by leading global investors and pharmaceutical,
technology, and healthcare companies. For more information, please
visit grail.com The Senior Scientist, Technical Operations is
responsible for supporting sustaining operations and introducing
new assays and diagnostic products into GRAIL’s high?throughput,
regulated laboratory environment. This individual contributor
partners closely with MSAT, Assay Development, Engineering
Operations, and the Clinical Lab to lead process integration,
improvement, monitoring, and troubleshooting. The ideal candidate
brings deep expertise across the end?to?end laboratory
workflow—from pre?analytical through post?analytical—strong process
optimization experience, and a thorough understanding of clinical
laboratory regulatory frameworks. This position is onsite full-time
, with 5 days per week at our facility. Additionally, the role
requires participation in a rotating schedule for weekend and
holiday coverage (when applicable) , as part of ensuring continuous
support for critical laboratory operations. Responsibilities: Lead
or assist in process troubleshooting activities, including
root-cause analysis and impact assessments, resolving technical
challenges. Monitor process performance, analyze data and metrics,
and contribute to process monitoring and improvement strategies to
sustain high-quality, efficient operations. Support the transfer
and implementation of new assays and diagnostic products from
development into production, ensuring robust performance across all
workflow phases. Develop, optimize, and document validation
protocols and procedures in compliance with CLIA, CAP, NYS, ISO
13485, FDA, and other applicable standards. Provide scientific and
technical support to MSAT, Engineering Operations, and Clinical Lab
teams. Evaluate, qualify, and implement alternative reagents and
vendors to maintain continuity and strengthen lab operations.
Identify process gaps and contribute to or lead process improvement
initiatives to enhance efficiency, reliability, and quality.
Prepare comprehensive technical documentation, scientific reports,
and regulatory submission materials as required. Maintain high
standards of scientific rigor, quality, and regulatory compliance
in all process integration activities. Lead complex investigations
and root-cause analyses; implement effective CAPAs and preventive
measures with clear verification of effectiveness. Support lab
readiness: training, tech transfer materials, troubleshooting
guides, and operational playbooks for Clinical Lab teams. Analyze
complex datasets and present insights to technical and
non-technical stakeholders to guide decisions. Contribute to
inspection/audit readiness and support interactions with CAP/CLIA,
state agencies (e.g., NYS), and other regulatory bodies as needed.
These responsibilities summarize the role’s primary
responsibilities and are not an exhaustive list. They may change at
the company’s discretion. Required Qualifications: PhD in Life
Sciences, Molecular Biology, Biochemistry, Bioengineering, or a
related field. Proven experience in technology transfer of assays
and launching new products in a regulated diagnostic laboratory.
Direct, hands-on experience with end-to-end clinical workflows
(pre-analytical, analytical, and post-analytical). Strong knowledge
of high-throughput laboratory automation and advanced
instrumentation. Deep understanding of clinical laboratory
regulatory standards, including CLIA, CAP, NYS, ISO 13485, and FDA.
Experience with or understanding of reagent manufacturing and
alternative vendor qualification processes. Experience
participating in audits (internal, regulatory, or client-driven).
Excellent skills in technical documentation and scientific writing.
Demonstrated ability to collaborate effectively across MSAT,
Engineering Operations, and Clinical Lab teams. Six Sigma
certification or significant experience with Lean, Kaizen, or other
process improvement methodologies. Hands-on experience with data
analytics tools and platforms (e.g., JMP, Minitab, R, Python,
Tableau) for process monitoring, analysis, and reporting.
Experience with laboratory information management systems (LIMS) or
MES. Advanced data analysis skills applied to laboratory operations
and quality improvement. Experience supporting laboratory scale-up,
automation, or operational excellence projects. Expected full time
annual base pay scale for this position is $119K - $142K. Actual
base pay will consider skills, experience and location. This role
may be eligible for other forms of compensation, including an
annual bonus and/or incentives, subject to the terms of the
applicable plans and Company discretion. This range reflects a
good-faith estimate of the range that the Company reasonably
expects to pay for the position upon hire; the actual compensation
offered may vary depending on factors such as the candidate’s
qualifications. Employees in this role are also eligible for
GRAIL’s comprehensive and competitive benefits package, offered in
accordance with our applicable plans and policies. This package
currently includes flexible time-off or vacation; a 401(k)
retirement plan with employer match; medical, dental, and vision
coverage; and carefully selected mindfulness programs. GRAIL is an
equal employment opportunity employer, and we are committed to
building a workplace where every individual can thrive, contribute,
and grow. All qualified applicants will receive consideration for
employment without regard to race, color, religion, national
origin, sex, gender, gender identity, sexual orientation, age,
disability, status as a protected veteran, , or any other class or
characteristic protected by applicable federal, state, and local
laws. Additionally, GRAIL will consider for employment qualified
applicants with arrest and conviction records in a manner
consistent with applicable law and provide reasonable
accommodations to qualified individuals with disabilities. Please
contact us at [email protected] if you require an accommodation to
apply for an open position. GRAIL maintains a drug-free workplace.
We welcome job-seekers from all backgrounds to join us!
Keywords: GRAIL Inc, Cary , Senior Scientist Technical Operations 4375, Science, Research & Development , Durham, North Carolina