Medical Director, Laboratory and Pathology

Veracyte

Location
South San Francisco, California, United States
Employment type
unknown
Posted
Posted
  • 205 Lab Testing COR Admin

About the role

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven environment. This is what we call the Veracyte way – it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions. Our Values: We Seek A Better Way : We pursue bold ideas, embrace complexity, and keep pushing forward. We Make It Happen : We act with urgency, deliver with excellence, and always find a way. We Are Stronger Together : We engage with empathy, align around what's best for Veracyte, and celebrate as one team. We Care Deeply : We show up with integrity, kindness, and respect for one another. The Position: The Medical 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 San Diego, 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: 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. <li style="font-family: arial,

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