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1 день назад

Senior Process Engineer (Oncology)

128 622 - 150 058$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Senior Process Engineer (Oncology) (Molecular Diagnostics): Developing and scaling clinical molecular diagnostic processes and assays for high-throughput oncology testing with an accent on process engineering, statistical analysis, data science, and GMP/ISO compliance. Focus on evaluating new technologies, validating chemistry and workflow changes, transferring processes into clinical production, and solving root-cause and scalability challenges.

Location: Onsite in Menlo Park, California, United States

Base pay: $128,622–$150,058 per year; total compensation up to $205,064 per year, including equity and bonus opportunities.

Company

hirify.global is a publicly traded molecular diagnostics company developing genomic tests for prenatal and cancer care using cell-free DNA and molecular counting technology.

What you will do

  • Lead the evaluation of external technologies that improve cost, throughput, assay performance, turnaround time, and operational metrics.
  • Develop process strategies supporting 2–3x annual growth in commercial testing volume.
  • Improve statistical process control, assay performance, failure rates, and process monitoring.
  • Lead technology transfer between R&D and the clinical laboratory, defining critical process parameters, tolerances, failure modes, and production workflows.
  • Work with Bioinformatics and Data Science to translate assay quality attributes into actionable monitoring tools and develop information-handling tools for sample processing.
  • Apply Six Sigma, Design for Quality, 5S, root-cause analysis, and related process-improvement methods while mentoring junior engineers.

Requirements

  • Bachelor’s, Master’s, or Ph.D. in biology, bioengineering, or a related science.
  • At least 5–6 years of experience with molecular biology techniques in a research or clinical laboratory.
  • Proficiency in R, Python, or an adjacent coding language, with strong statistical analysis and experimental design skills.
  • Experience designing controlled molecular biology studies, presenting data, and authoring technical reports.
  • Experience in GMP, ISO, or equivalent environments, with strong knowledge of quality management systems and practices.
  • Strong troubleshooting, communication, attention to detail, and junior-team mentoring skills.

Nice to have

  • Startup experience and knowledge of medical genetics or cell-free DNA.
  • Experience with Six Sigma, Lean, JIT, or TPS.
  • Experience with CLIA/CAP, 510(k), PMA, automation, or clinical laboratory operations.

Culture & Benefits

  • Open, transparent, collaborative environment with weekly town halls.
  • Medical benefit options, including fully paid employee premiums for select plans and dependent coverage.
  • Sixteen weeks of fully paid family bonding leave for eligible employees and supplemental fertility benefits.
  • Retirement savings program with a 4% company match and increasing paid time off based on tenure.
  • Onsite lunches, campus amenities, modern laboratory equipment, and free EV charging.

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