Veracyte

Director, Laboratory and Pathology

Veracyte$300K — $350K *
Healthcare
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • MD, DO, or DPM; licensed to practice in California; certified in anatomic pathology.
  • Fellowship in Molecular Pathology is required.
  • NY Certificate of Qualification in Oncology, Molecular and Cellular Tumor Markers required.
  • 10+ years of experience in a CAP/CLIA-accredited and/or New York State-licensed clinical laboratory.
  • Ability to work a Tuesday through Saturday schedule.

Responsibilities

  • Direct and oversee laboratory operations for accurate, timely diagnostic services.
  • Provide medical and scientific oversight of histology workflows.
  • Review H&E-stained slides and assess tissue adequacy and specimen quality.
  • Provide consultation on diagnostic interpretation and tissue handling.
  • Ensure compliance with CLIA, CAP, NY state, and other regulations.
  • Participate in audits and address findings appropriately.
  • Monitor laboratory performance, turnaround time, and safety conditions.

Benefits

  • Opportunity for leadership in a key laboratory role.
  • Participation in implementing new technologies and process improvements.
  • Collaborative work environment with a focus on patient-centered quality.
  • Quarterly travel to San Diego for business meetings.
  • Potential for additional bonuses and stock options.
Full Job Description
The Position:

The Director, Laboratory and Pathology is accountable for the overall operation, administration, quality, and regulatory compliance of the South San Francisco laboratory, ensuring accurate, timely, and reliable laboratory services and appropriately qualified personnel.

This is an onsite role based out of our South San Francisco, CA office with a schedule of Tuesday-Saturday.

Responsibilities:
  • Direct and oversee laboratory operations to provide high-quality, accurate, and timely diagnostic services.
  • Provide medical and scientific oversight of histology workflows, including tissue processing, embedding, microtomy, H&E staining, special stains, and immunohistochemistry.
  • Review H&E-stained slides; assess tissue adequacy, morphology, tumor content, and specimen quality for diagnostic and molecular testing.
  • Provide consultation on diagnostic interpretation, specimen triage, tissue handling, fixation, acceptance criteria, test utilization, and reported results.
  • Ensure compliance with applicable CLIA, CAP, NY state, and other regulatory requirements.
  • Participate in inspections and audits and ensure findings are addressed.
  • Oversee testing systems across pre-analytic, analytic, and post-analytic phases, including method selection, verification, validation, performance monitoring, and report content.
  • Ensure proficiency testing, quality control, quality assessment, and corrective action programs are established, maintained, reviewed, and documented.
  • Ensure personnel are appropriately qualified, trained, authorized, and competent, with responsibilities defined in writing and current procedures available.
  • Guide and mentor laboratory leaders and staff; delegate qualified responsibilities as appropriate while retaining accountability for their performance.
  • Monitor laboratory performance, turnaround time, workflow, budget, safety, environmental conditions, and reference laboratory selection.
  • Lead implementation of new technologies and process improvements, collaborate across disciplines, and remain accessible for onsite, telephone, or electronic consultation.
Who You Are:
  • A collaborative medical and scientific leader with strong clinical judgment and a commitment to patient-centered laboratory quality.
  • Skilled at leading, mentoring, and working effectively with pathologists, clinicians, laboratory personnel, and cross-functional partners.
  • Able to translate regulatory and quality requirements into clear, practical laboratory practices.
  • Able to maintain effective working relationships with applicable accrediting and regulatory agencies, administrative officials, and the medical community.
  • A clear communicator who can provide sound consultation, align stakeholders, and support timely decisions.
  • Analytical and improvement-oriented, with the ability to evaluate performance, identify risk, and advance efficient, reliable workflows.
  • Accountable, accessible, and adaptable in a changing clinical laboratory environment.
  • Able to travel to the San Diego office on a quarterly basis to attend business related meetings.

Required Qualifications:
  • MD, DO, or DPM; licensed to practice in California; and certified in anatomic pathology by the American Board of Pathology or American Osteopathic Board of Pathology.
  • Fellowship in Molecular Pathology is required.
  • NY Certificate of Qualification in Oncology, Molecular and Cellular Tumor Markers required
  • 10+ years of experience in a CAP/CLIA-accredited and/or New York State-licensed clinical laboratory.
  • This role is expected to work a Tuesday through Saturday schedule to support Laboratory Operations in South San Francisco, CA.

The responsibilities above are representative and may include other duties consistent with the role and applicable regulatory requirements.

#LI-Onsite

The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to years of experience, skillset, geographic location, industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units.

Pay range

$300,000-$350,000 USD

What We Can Offer You

About Veracyte

Veracyte is a genomic diagnostics company that uses advanced genomic technology to resolve diagnostic uncertainty and deliver actionable results that improve patient care and outcomes. The company's tests in thyroid, lung, and breast cancer, and in idiopathic pulmonary fibrosis, are becoming standard of care in helping patients avoid unnecessary invasive procedures, while resolving inconclusive results from traditional diagnostic methods. Veracyte's genomic tests are covered by Medicare and many commercial insurance plans. With Veracyte's exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide. The company was founded in 2008 and is headquartered in South San Francisco, California.
Learn more about Veracyte
Size
761 employees
Market Cap
$1.8 billion
Industry
Net Income
-$34.9 million
Founded
2006
5 Year Trend
+27.5%
Revenue
$117.4 million
NASDAQ

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