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9 дней назад

US MDM and Supply Chain Operations Specialist

Формат работы
onsite
Тип работы
fulltime
Грейд
middle
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:
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TL;DR
US MDM and Supply Chain Operations Specialist (SAP/Supply Chain): Managing SAP S/4HANA master data and supply chain operations across the R&D to GMP lifecycle with an accent on material master creation, data integrity, SUT logistics, and external warehouse coordination. Focus on executing UAT, improving system workflows, supporting RFID deployment, and ensuring cGMP-compliant operational processes.

Location: Waltham, Massachusetts, United States; onsite

Company

hirify.global is an R&D-driven, AI-powered biopharmaceutical company developing medicines and vaccines through science, mRNA innovation, and advanced manufacturing.

What you will do

  • Act as a key user and subject matter expert for SAP S/4HANA Supply Chain modules, supporting users and troubleshooting routine issues.
  • Create and maintain Material Masters, bills of materials, resources, and technical planning parameters across the R&D to GMP lifecycle.
  • Coordinate system flows, user acceptance testing, patches, upgrades, and continuous improvement initiatives.
  • Support Single-Use Technologies inventory coordination, receiving verification, outbound shipment preparation, and external 3PL warehouse alignment.
  • Support RFID tracking deployment, procurement and GMP receiving issue resolution, labeling verification, and local user training.

Requirements

  • Bachelor’s degree required; a master’s degree in Supply Chain Management, Information Systems, Business, Engineering, or a related discipline is preferred.
  • At least 4 years of relevant supply chain experience, preferably in pharmaceutical, biotech, healthcare, life sciences, or a related industry.
  • Hands-on experience with SAP S/4HANA or ECC Supply Chain and Master Data modules, including material masters, bills of materials, and master records.
  • Understanding of cGMP regulations, ALCOA+ data integrity principles, MRP parameters, and lifecycle management from development through GMP stages.
  • Strong attention to detail, problem-solving, communication, and cross-functional collaboration skills.
  • Onsite work in Waltham, Massachusetts, United States is required.

Culture & Benefits

  • Work alongside a science-focused team advancing vaccines, mRNA platforms, AI-driven research, and smart manufacturing.
  • Career development opportunities through promotions, lateral moves, mentoring, and international mobility programs.
  • Employee rewards, healthcare, prevention and wellness programs, and at least 14 weeks of gender-neutral parental leave.
  • Contribute to a global vaccination effort protecting hundreds of millions of people each year.

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