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6 дней назад

CMC Demand & Supply Leader

122 250 - 176 583$
Формат работы
onsite
Тип работы
fulltime
Грейд
lead
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
CMC Demand & Supply Leader (Biopharma): Integrating project strategy, clinical plans, and CMC operations to forecast and optimize end-to-end demand and supply for R&D and clinical development programs with an accent on regulated pharmaceutical supply planning, sourcing strategy, and risk-cost analysis. Focus on consolidating clinical and non-clinical demand, aligning supply scenarios with regulatory plans, and ensuring drug product allocation and delivery for clinical trials.

Location: Framingham, Massachusetts, United States; onsite

Salary: $122,250–$176,583.33 per year

Company

hirify.global is an R&D-driven, AI-powered biopharmaceutical company developing medicines and vaccines across multiple therapeutic areas.

What you will do

  • Lead collaboration with project management, clinical development, and CMC stakeholders to define clinical assumptions and forecast demand.
  • Consolidate non-clinical and clinical demand and align development requirements with global supply chain operations.
  • Integrate CMC, clinical, operational, and regulatory submission plans into end-to-end demand and supply strategies.
  • Run demand and supply scenarios covering risks, costs, budgets, sourcing, and supply optimization.
  • Define blinding strategies and allocate drug substance and drug product batches to investigational medicinal product batches.
  • Monitor supply performance through KPIs and manage delivery, material flow, documentation, and project reporting.

Requirements

  • PhD, MS, or BS in a relevant scientific, life sciences, pharmaceutical, chemical engineering, or biomedical engineering discipline.
  • At least 3 years of R&D or clinical development experience with a PhD, 5 years with an MS, or 8 years with a BS.
  • At least 2 years of R&D demand management experience in oncology, immuno-inflammation, rare disease, neurology, or multiple sclerosis.
  • CMC experience and the ability to work in complex regulated environments governed by GMP and GCP requirements.
  • Knowledge of data analytics and forecasting, plus project management experience.
  • Applicants must be located in the United States; this is an onsite role in Framingham, Massachusetts.

Nice to have

  • Experience with mammalian, genomic, microbial, or synthetic modalities and clinical supply chain interfaces.
  • PMI certification and experience with Power BI, Power Apps, or project management software.
  • Experience with co-development projects, company integrations, contract management, and industrial supply chain principles.
  • Team management experience and strong transversal collaboration skills.

Culture & Benefits

  • Supportive, future-focused environment centered on science, innovation, and patient impact.
  • Opportunities for career growth through promotion or lateral moves.
  • Health, wellbeing, prevention, and wellness programs.
  • At least 14 weeks of gender-neutral parental leave.
  • Work with AI, data, and digital platforms supporting drug discovery and development.

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