Назад
Company hidden
2 часа назад

Principal Scientist, Bioanalytical & Molecular Assays (Genomics)

Формат работы
hybrid
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
UK
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
/
TL;DR
Principal Scientist, Bioanalytical & Molecular Assays (Genomics): Developing and validating molecular assays, including RT-qPCR, dPCR, and NGS, to support clinical endpoints across therapeutic programs with an accent on assay lifecycle ownership, clinical sample testing, and regulatory compliance. Focus on building bioinformatics pipelines, integrating genomics data with laboratory systems, and translating complex molecular findings into actionable clinical development recommendations.

Location: hirify.global’s Harwell site, United Kingdom; 70% in-office under a 70/30 work model

Company

hirify.global develops mRNA medicines and technologies to transform how medicines are created and delivered.

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 from method development and qualification through validation, clinical sample testing, reporting, and technology transfer to laboratories and CRO partners.
  • Ensure assay quality, reproducibility, scalability, data integrity, inspection readiness, and alignment with regulatory expectations.
  • Provide scientific subject-matter expertise and matrix leadership across molecular biology, NGS, bioinformatics, clinical development, regulatory, quality, data, and IT teams.
  • Translate molecular and genomic data into clinical development recommendations and identify scientific opportunities for the future pipeline.

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 end-to-end workflows.
  • Experience with library preparation, nucleic acid extraction from diverse matrices, and orthogonal QC using Bioanalyzer, TapeStation, qPCR, or dPCR.
  • Demonstrated experience building and validating bioinformatics pipelines.
  • Knowledge of GCLP/GLP, GxP, MHRA, and ICH expectations, phase-appropriate clinical validation, deviation investigations, CAPA, and inspection readiness.
  • Experience integrating genomics data and instrumentation with LIMS/ELN, data governance, and secure clinical-data handling.

Culture & Benefits

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

Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →