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4 дня назад

Principal Scientist, Bioanalytical & Molecular Assays (Genomics)

Формат работы
hybrid
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
UK/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
Principal Scientist, Bioanalytical & Molecular Assays (Genomics): Developing, validating, and deploying RT-qPCR, dPCR, and NGS-based molecular assays for clinical biomarker and endpoint programs with an accent on assay lifecycle ownership, genomic workflows, and regulatory-quality data. Focus on leading clinical sample testing, building bioinformatics pipelines, managing validation and technology transfer, and translating complex molecular data into actionable development decisions.

Location: hirify.global’s Harwell site in Oxford, England; 70% in-office work model

Company

hirify.global develops mRNA-based therapeutics and vaccines across infectious diseases, immuno-oncology, rare diseases, and cardiovascular diseases.

What you will do

  • Lead the design, development, optimization, validation, and delivery of molecular assays supporting clinical endpoints.
  • Develop and implement RT-qPCR, dPCR, and NGS assays for gene expression, viral load, mRNA pharmacokinetics, RNA sequencing, single-cell sequencing, immune repertoire profiling, targeted DNA panels, and pathogen sequencing.
  • Own end-to-end assay lifecycle activities, including method development, qualification, validation, clinical sample testing, reporting, and technology transfer to internal laboratories and CRO partners.
  • Oversee quality control, data integrity, deviation investigations, CAPA activities, and inspection-readiness efforts.
  • Provide scientific subject matter expertise and matrix leadership across clinical development programs from Phase 1 through Phase 3.
  • Partner with Clinical Development, Biomarkers, Translational Medicine, Bioanalytics, Regulatory Affairs, Quality Assurance, Data, and IT teams to translate molecular and genomic data into program decisions.

Requirements

  • Ph.D. in Molecular Biology, Genomics, or a related field with 9+ years of biotech or pharma experience, or an M.S. with 12+ years of directly relevant experience.
  • Hands-on experience developing and validating clinical qPCR, dPCR, and NGS assays across complete workflows.
  • Knowledge of GCLP/GLP, GxP, MHRA, and ICH expectations, phase-appropriate validation, and inspection readiness.
  • Experience with library preparation, nucleic acid extraction, Bioanalyzer or TapeStation, qPCR/dPCR, and orthogonal quality control.
  • Track record of building and validating bioinformatics pipelines and integrating genomics data and instrumentation with LIMS/ELN and data governance systems.
  • Ability to work independently, lead multidisciplinary teams, mentor colleagues, and communicate complex scientific strategies to technical and non-technical stakeholders.

Culture & Benefits

  • Collaborative, fast-moving environment focused on scientific rigor, innovation, and patient impact.
  • Healthcare and voluntary benefit programs, plus fitness, mindfulness, and mental health support.
  • Family-building support, including fertility, adoption, and surrogacy benefits.
  • Paid vacation, bank holidays, volunteer days, sabbatical, global recharge days, and year-end shutdown.
  • Savings and investment programs and location-specific benefits.

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