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22 часа назад

Principal Scientist, Bioanalytical & Molecular Assays

Формат работы
hybrid
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
UK
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 (Molecular Biology/Genomics): Developing, validating, and deploying advanced molecular assays including qPCR, dPCR, and NGS workflows to generate clinical biomarker data across therapeutic programs with an accent on assay robustness, regulatory compliance, and translational insights. Focus on building bioinformatics pipelines, managing end-to-end assay lifecycles, interpreting complex genomic data, and leading cross-functional scientific decision-making from Phase 1 through Phase 3.

Location: Oxford, England; based at hirify.global’s Harwell site with a 70/30 in-office work model

Company

hirify.global develops mRNA medicines and technologies to advance treatments and transform medicine.

What you will do

  • Lead the design, development, optimization, validation, and deployment of molecular assays supporting clinical endpoints.
  • Develop RT-qPCR, dPCR, and NGS assays for gene expression, viral load, mRNA pharmacokinetics, RNA sequencing, immune repertoire profiling, targeted DNA panels, and pathogen sequencing.
  • Own assay lifecycle activities, including method development, qualification, validation, clinical sample testing, reporting, and technology transfer to internal laboratories and CRO partners.
  • Prepare and review validation plans, protocols, reports, acceptance criteria, and technical documentation in accordance with GCLP requirements.
  • Lead deviation investigations, CAPA activities, quality oversight, inspection readiness, and audit preparedness.
  • Provide scientific leadership across multidisciplinary teams and translate molecular and genomic data into actionable clinical development recommendations.

Requirements

  • Ph.D. in Molecular Biology, Genomics, or a related field with 9+ years of biotech or pharmaceutical 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 the full workflow from method development through reporting.
  • Knowledge of GCLP/GLP, GxP, MHRA, and ICH expectations, phase-appropriate clinical validation, and inspection readiness.
  • Experience with library preparation, nucleic acid extraction from diverse matrices, and orthogonal QC using Bioanalyzer, TapeStation, qPCR, or dPCR.
  • Track record of building and validating bioinformatics pipelines.
  • Experience integrating genomics data and instrumentation with LIMS/ELN, data governance, and secure clinical data handling.

Culture & Benefits

  • In-person collaboration supported by a 70/30 in-office work model.
  • Healthcare coverage and voluntary benefit programs.
  • Fitness, mindfulness, and mental health resources.
  • Family-building support, including fertility, adoption, and surrogacy benefits.
  • Paid vacation, bank holidays, volunteer days, sabbatical, global recharge days, and discretionary year-end shutdown.
  • Savings and investment programs plus location-specific benefits.

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