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5 дней назад

Manager, Materials Management (Biotech)

125 000 - 165 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
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
Manager, Materials Management (Biotech): Leading end-to-end materials operations for clinical and commercial manufacturing, including receiving, storage, inventory control, GMP pack-out, and shipping with an accent on compliance, chain of custody, and operational efficiency. Focus on managing materials teams, validating warehouse systems, coordinating 3PL providers, and improving material flow across cleanroom and manufacturing environments.

Location: Waltham, Massachusetts, United States

Salary: $125,000–$165,000 per year

Company

hirify.global is a technology-driven biotechnology company developing and manufacturing advanced therapies from design through commercialization.

What you will do

  • Lead receiving, inventory control, kitting, material issuance, storage, and GMP pack-out operations.
  • Oversee shipping of drug substance and drug product, including chain of custody and documentation compliance.
  • Manage cycle counting, inventory accuracy, warehouse systems, equipment requirements, and validation activities.
  • Lead and develop materials specialists and leads while ensuring operational flexibility and GMP compliance.
  • Manage third-party logistics providers, including service levels, scheduling, documentation, and cost control.
  • Drive cross-functional investigations and continuous improvement initiatives across manufacturing, quality, validation, and facilities.

Requirements

  • Bachelor’s degree with at least 6 years of related experience, or a Master’s degree with at least 4 years, or a PhD with at least 2 years.
  • People management or leadership experience.
  • Expertise with SAP or similar ERP inventory systems.
  • Experience with Veeva, Kneat, and BM-RAM quality and validation systems.
  • Strong understanding of GMP regulations, chain of custody, and materials flow in clinical and commercial manufacturing.
  • Ability to perform extended periods of standing, walking, bending, stretching, lifting 15–20 pounds, and working with PPE.

Culture & Benefits

  • Regular employment within the Supply Chain department.
  • Cross-functional work with Manufacturing, Quality, Validation, and Facilities.
  • Focus on operational excellence, compliance, waste reduction, and continuous improvement.
  • Work in cleanroom and manufacturing environments with required personal protective equipment.

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