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14 часов назад

Analytical Sciences Director

Формат работы
hybrid
Тип работы
fulltime
Грейд
director
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
Analytical Sciences Director (Pharmaceutical R&D/CMC): Leading analytical sciences for synthetic small-molecule and solid oral dosage-form development in Cambridge with an accent on advanced analytical strategies, regulatory support, and laboratory digitalization. Focus on building scientific capabilities, managing cross-functional resources, advancing analytical technologies, and developing high-performing teams across clinical and commercial programs.

Location: Hybrid role in Cambridge, Massachusetts, United States

Company

hirify.global develops synthetic small-molecule medicines and oral drug products from candidate selection through clinical manufacturing, regulatory submission, and product approval.

What you will do

  • Lead analytical sciences activities for synthetic small molecules and solid oral dosage forms at the Cambridge Crossing site.
  • Develop and apply analytical strategies, technologies, and control approaches across drug substance and drug product development.
  • Support process chemistry, pre-formulation, stability studies, clinical documentation, and regulatory dossier preparation.
  • Lead analytical sciences digital transformation, laboratory automation, technology upgrades, and external scientific collaborations.
  • Allocate resources, oversee outsourced activities, review scientific documents, and provide transversal support across CMC functions.
  • Manage, coach, and develop a team of high-level scientists while representing Analytical Sciences internally and externally.

Requirements

  • BS in Analytical Chemistry or a related field with at least 14 years of relevant pharmaceutical industry experience; or MS with at least 12 years; or PhD with at least 10 years.
  • At least 3 years of demonstrated people management and leadership experience.
  • Strong knowledge of pharmaceutical regulatory requirements, including GMP, ICH guidelines, pharmacopoeia, and EMA/FDA regulations.
  • Experience with clinical trial documentation, CTD submissions, and regulatory dossier preparation.
  • Strong R&D track record in analytical sciences, an established scientific network, and experience managing high-level scientists in a matrix organization.
  • English is required.

Culture & Benefits

  • Supportive, future-focused environment centered on scientific innovation.
  • Career growth opportunities through promotion or lateral and international moves.
  • Rewards package linked to contribution and impact.
  • Healthcare, prevention, and wellness benefits for employees and families.
  • At least 14 weeks of gender-neutral parental leave.

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