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5 дней назад

Lead Scientist (Bioanalysis)

Формат работы
onsite
Тип работы
fulltime
Грейд
lead
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
Lead Scientist (Bioanalysis/LC-MS/MS): Leading bioanalytical method development, validation, and regulated study activities in a CRO environment with an accent on scientific oversight, client coordination, and regulatory compliance. Focus on managing complex studies, resolving assay and scientific challenges, and mentoring scientific staff while meeting GLP, GCP, quality, and timeline requirements.

Location: Harrogate, United Kingdom; onsite at hirify.global's UK site.

Company

Global laboratory services provider supporting healthcare, pharmaceutical, research, and diagnostic organizations through science, data, technology, and laboratory services.

What you will do

  • Lead bioanalytical LC-MS/MS method development, validation, sample analysis, and study activities.
  • Serve as Study Director, Principal Investigator, or Responsible Scientist for regulated and non-regulated studies.
  • Develop, review, and approve protocols, validation plans, reports, and study data.
  • Provide scientific oversight for GLP, GCP, regulatory, and client requirements.
  • Act as the primary scientific contact for clients, managing project requirements, expectations, risks, and scope changes.
  • Lead, mentor, and develop scientific staff while managing multiple complex projects and continuous improvement initiatives.

Requirements

  • Bachelor's degree or equivalent experience in a relevant scientific discipline.
  • Significant experience in bioanalytical method development, validation, and regulated study conduct within a Contract Research Organization environment.
  • Previous experience as a Study Director, Principal Investigator, and/or Responsible Scientist for regulated bioanalytical studies.
  • Thorough understanding of GLP, GCP, and global regulatory requirements for bioanalytical studies.
  • Strong scientific data interpretation, technical troubleshooting, regulatory decision-making, client management, and stakeholder engagement skills.
  • Leadership, mentoring, and project management experience with the ability to manage high-volume workloads while maintaining quality and compliance.

Culture & Benefits

  • Work in a science-focused laboratory environment supporting healthcare and pharmaceutical research.
  • Collaborate with clients and scientific teams on studies of varying complexity.
  • Contribute to initiatives focused on scientific excellence, quality, and client satisfaction.
  • Equal opportunity workplace committed to inclusion and belonging.

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