Назад
Company hidden
2 дня назад

Analytical Sciences Director (Pharmaceutical R&D)

178 500 - 257 833$
Формат работы
hybrid
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
US
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
Analytical Sciences Director (Pharmaceutical R&D): Leading analytical sciences for synthetic small-molecule and solid oral dosage-form development with an accent on advanced analytical strategies, regulatory support, and laboratory digitalization. Focus on developing analytical technologies, managing cross-functional scientific teams, and supporting CMC programs from early development through clinical dossier submission.

Location: Cambridge, Massachusetts, United States; hybrid

Salary: $178,500–$257,833.33 per year

Company

hirify.global develops pharmaceutical products and supports synthetic small-molecule drug development from candidate selection through regulatory 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 advanced analytical strategies for First in Class and Best in Class R&D programs.
  • Support process chemistry, pre-formulation, control strategy development, and stability studies across intermediates, starting materials, drug substance, and drug product.
  • Lead analytical technology innovation, laboratory digitalization, automation, and intellectual property generation.
  • Allocate resources, oversee outsourced activities, review scientific documents, and support CMC development projects.
  • Manage, coach, develop, and empower a cross-functional Analytical Sciences team.

Requirements

  • BS in Analytical Chemistry or a related field with at least 14 years of 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 ICH guidelines, EMA/FDA regulations, GMP, and pharmacopoeia.
  • Experience with clinical trial documentation, clinical dossiers, CTD submissions, and regulatory filings.
  • Strong R&D track record in analytical sciences and experience managing teams of high-level scientists.
  • English is required.

Culture & Benefits

  • Supportive, future-focused environment centered on scientific innovation.
  • Opportunities for promotion, lateral career moves, and international development.
  • Rewards package aligned with contribution and impact.
  • Healthcare, prevention, and wellness programs.
  • At least 14 weeks of gender-neutral parental leave.

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 →