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4 дня назад

Senior Director, Supply Chain (Pharmaceutical Manufacturing)

211 000 - 330 000$
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

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TL;DR
Senior Director, Supply Chain (Pharmaceutical Manufacturing): Leading end-to-end supply chain planning and operations for a biologics manufacturing site with an accent on supply planning, capacity management, inventory optimization, compliance, and cross-functional leadership. Focus on building scalable planning processes, solving capacity and operational risks, and driving continuous improvement across SAP, OMP, warehousing, logistics, and manufacturing programs.

Location: US - Vacaville, California

Salary: $211,000.00–$330,000.00 per year in base pay

Company

hirify.global is a global life sciences company providing products and services for pharmaceutical and biologics manufacturing.

What you will do

  • Lead end-to-end supply planning, master production scheduling, capacity planning, and S&OP for the Vacaville manufacturing site.
  • Develop supply, capacity, and prioritization scenarios to optimize asset utilization, customer service, and operational performance.
  • Oversee inventory planning, material flow, warehousing, logistics, and planning-system data across SAP, OMP, and related tools.
  • Partner with Manufacturing, Quality, MSAT, Engineering, Finance, Commercial, Procurement, IT, Network Planning, and Program Management.
  • Prepare supply chain planning and scheduling for capital projects, operational start-up, and ramp-up.
  • Lead transformation, KPI reporting, continuous improvement, and development of the Supply Planning and Scheduling team.

Requirements

  • Bachelor’s degree in Supply Chain, Business Administration, Industrial Engineering, Natural Sciences, or a related field; a master’s degree is preferred.
  • At least 10 years of progressive supply chain experience in a manufacturing environment; pharmaceutical manufacturing or CDMO experience is strongly preferred.
  • Experience leading compliant end-to-end supply chain operations, including planning, procurement, data management, warehousing, and logistics under GxP requirements.
  • Ability to manage quality and EHS risks, establish KPIs, perform root cause analysis, and lead continuous improvement.
  • Strong cross-functional leadership, analytical, problem-solving, communication, and decision-making skills.
  • Proficiency with business intelligence tools and Microsoft Office, especially Excel and PowerPoint.

Culture & Benefits

  • Full-time employment with performance-related bonus eligibility.
  • Medical and dental coverage, 401k plan, life insurance, and short- and long-term disability insurance.
  • Employee assistance program and paid time off.
  • Work focused on ethical, compliant, and environmentally responsible life sciences operations.
  • Equal opportunity employment.

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