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Senior Director, Global Manufacturing Programs

200 812 - 286 157$
Формат работы
onsite
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
Senior Director, Global Manufacturing Programs (Pharmaceutical Manufacturing): Leading end-to-end technical delivery for global manufacturing programs, including MedSuRe, with an accent on technology transfer, scale-up, process validation, and regulatory pathways. Focus on integrating concurrent workstreams, managing technical risks and dependencies, and guiding geographically dispersed matrixed teams toward measurable program outcomes.

Location: Rockville, Maryland, United States

Base salary: USD $200,812–$286,157 annually. Target annual bonus: 13%, varying by role level.

Company

hirify.global is an independent scientific nonprofit organization that develops public standards and programs to strengthen the global supply of safe, high-quality medicines.

What you will do

  • Provide end-to-end technical leadership for MedSuRe and other global manufacturing programs.
  • Set technical direction, governance frameworks, standards, and best practices across matrixed teams.
  • Translate organizational and donor strategies into integrated program plans, milestones, and resource requirements.
  • Monitor delivery, quality, performance, risks, and dependencies across concurrent technical workstreams.
  • Represent USP in engagements with donors, partners, and external stakeholders, including technical reviews and proposal development.
  • Lead and mentor multidisciplinary, geographically dispersed teams while strengthening accountability and technical capability.

Requirements

  • Advanced degree, such as a Ph.D. or MS, in Pharmaceutical Sciences, Chemistry, Public Health, or a related field.
  • At least 12 years of experience, including leadership experience in pharmaceutical, biotech, or advanced manufacturing environments.
  • Deep understanding of drug development and commercialization, manufacturing processes, technology transfer, scale-up, process validation, and regulatory approval pathways.
  • Experience leading complex programs or portfolios with technical risk, dependencies, and multiple concurrent workstreams.
  • Strong cross-functional leadership, stakeholder management, executive communication, conflict resolution, and alignment-building skills.
  • Understanding of operating contexts and challenges in low- and middle-income countries is valued.

Culture & Benefits

  • Company-paid time off and comprehensive healthcare options.
  • Retirement savings benefits.
  • Inclusive, diverse, and collaborative work environment.
  • Opportunities to work with experts from industry, academia, healthcare, and government.
  • Work focused on global health, public scientific standards, and access to safe, quality medicines.

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