12 дней назад
US MDM and Supply Chain Operations Specialist (SAP)
71 250 - 102 916$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
US MDM and Supply Chain Operations Specialist (SAP): Executing SAP S/4HANA master data operations and supporting supply chain workflows across the R&D to GMP lifecycle with an accent on material masters, BOMs, data integrity, and SUT logistics. Focus on configuring and validating end-to-end operational flows, coordinating UAT, supporting external warehouses, and maintaining RFID tracking in regulated biopharma operations.
Location: Waltham, Massachusetts, United States; onsite
Salary: $71,250.00–$102,916.66 per year
Company
is an R&D-driven biopharmaceutical company developing medicines and vaccines through mRNA innovation, AI-driven research, and immunology platforms.
What you will do
- Serve as a key user and subject matter expert for SAP S/4HANA Supply Chain modules, including Planning, Procurement, and EWM.
- Create and maintain Material Masters, Bills of Materials, Resources, and technical planning parameters across the R&D to GMP lifecycle.
- Execute and monitor end-to-end system flows involving internal manufacturing sites and external partners.
- Coordinate User Acceptance Testing for new features, patches, and global SAP upgrades.
- Support Single-Use Technologies inventory coordination, receiving verification, outbound shipment preparation, and external 3PL warehouse alignment.
- Support SAP workflow standardization, procurement and GMP receiving issues, RFID deployment, and 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 operations 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.
- Experience managing Material Masters, BOMs, master records, MRP parameters, and lifecycle transitions.
- Understanding of cGMP regulations and ALCOA+ data integrity principles in a regulated biopharmaceutical environment.
- Strong attention to detail, troubleshooting, collaboration, communication, and user training skills.
Culture & Benefits
- Work alongside teams focused on mRNA innovation, AI-driven research, smart manufacturing, and immunology.
- Career growth opportunities through promotions, lateral moves, mentoring, and international mobility programs.
- Employee rewards and benefits, including healthcare, prevention and wellness programs.
- At least 14 weeks of gender-neutral parental leave.
- Opportunity to contribute to a global vaccination effort protecting hundreds of millions of people.
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