Jobs / United States / Elevatebio Technologies INC
Manager, Materials Management
Elevatebio Technologies INC · 🇺🇸 Waltham, Massachusetts, United States
Sponsorship verdict
Sponsorship possible
One solid signal, not two — worth applying, and worth asking about sponsorship early.
- Employer is on a government sponsor recordThe US Department of Labor certified 11 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first. USCIS also records 1 H-1B approvals in FY2023. Source: LCA disclosure data (US Department of Labor (OFLC)).
- The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
- No salary bar for this routeH-1B has no fixed salary bar: the employer must pay at least the prevailing wage for the role and area. Cap-subject employers enter a lottery weighted by wage level. Source: https://www.federalregister.gov/documents/2025/12/29/2025-23853/weighted-selection-process-for-registrants-and-petitioners-seeking-to-file-cap-subject-h-1b, rules effective 2026-02-27.
- Confirmed live todayWhen a source last listed this job as open.
US H-1B: cap-subject employers enter a lottery weighted by wage level — Level I gets 1 entry, Level IV gets 4 (DHS projected selection odds ≈15% at Level I to ≈61% at Level IV). Universities and non-profit research employers are cap-exempt. The $100,000 fee for new petitions from abroad is currently blocked by a court order (appeal pending).
A verdict summarises public evidence; it is not legal advice and never a guarantee — the employer and the immigration authority decide. Sign in to factor in where you can already work.
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Sponsor Radar — Elevatebio Technologies INC
The US Department of Labor certified 11 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first. USCIS also records 1 H-1B approvals in FY2023. Source: LCA disclosure data (US Department of Labor (OFLC)).
Past sponsorship or register membership never guarantees sponsorship for this vacancy or for you. Full Sponsor Radar for Elevatebio Technologies INC →
About the role
ElevateBio is a technology-driven company powering the industry forward by helping partners realize the potential of their therapies from design to commercialization. We have integrated a differentiated set of technologies, end-to-end services, and industry-leading manufacturing expertise to develop advanced therapies faster and more efficiently. The Role ElevateBio is seeking a Manager, Materials Management to lead and oversee end-to-end materials operations at our manufacturing facility. This highly visible and strategic role is accountable for ensuring compliant, timely, and efficient handling of raw materials, patient-derived materials, manufacturing intermediates, drug substance, and drug product. The Manager will own and direct material receipts, storage, issuance, and final pack-out while also overseeing inventory control, warehouse systems, and third-party logistics. This leader will collaborate cross-functionally with Manufacturing, Quality, Validation, and Facilities, serving as a key interface for operational excellence, compliance, and continuous improvement in support of ElevateBio’s manufacturing network. Here’s What You’ll Do • Lead daily operations for materials handling including receiving, inventory control, kitting, and material issuance to manufacturing • Oversee GMP pack-out and shipping of drug substance and drug product, ensuring chain of custody and documentation compliance • Manage the cycle count program and drive inventory accuracy for both inventoried and non-inventoried materials • Develop and maintain user requirements and business cases for warehouse equipment, infrastructure, and systems • Serve as a people leader, coaching and developing a team of materials specialists and leads, ensuring flexibility, performance, and GMP compliance • Act as the key contact for third-party logistics (3PL) providers, managing service levels, documentation, scheduling, and cost control • Support budgeting for materials operations and approve invoices related to shipping, compressed gases, 3PL services, etc. • Lead or contribute to cross-functional projects that improve inventory control, reduce waste, or optimize operational workflows • Execute, manage, and approve quality records in Veeva for SOP creation/revisions, deviations, CAPAs, and change controls • Own materials management validation activities within Kneat, including protocol execution and approval of validation documentation • Champion best practices for controlled material flow, gowning materials, and operational support inventory across cleanroom areas • Lead cross-functional investigations and improvements related to material movement, storage conditions, and supply support for clinical manufacturing Requirements • Bachelor’s degree and at least 6 years of related experience, OR Master’s degree with at least 4 years of related experience, OR PhD with at least 2 years of experience. • People management or leadership experience • Expertise in SAP or similar ERP inventory systems • Proficiency in quality and validation systems such as Veeva, Kneat, and BM-RAM • Strong understanding of GMP regulations, chain of custody principles, and materials flow in clinical and commercial manufacturing environments • Experience working with 3PL providers and managing shipping/receiving of high-value materials • Excellent communication, organizational, and analytical skills • Demonstrated ability to lead cross-functional initiatives and continuous improvement projects Physical and Environment Requirements: • Ability to stand, walk, bend and stretch for extended period of time • Ability to lift 15-20 lbs • Ability to push, pull, bend, kneel, twist and climb step ladders while wearing PPE. • Ability to perform routine repetitive motions with u