---
title: 'Manager, Materials Management at ElevateBio'
canonical: 'https://feeny.ai/job/manager-materials-management-elevatebio-waltham-aedqw9k69be1'
type: 'job'
last_seen: '2026-10-16'
---

# Manager, Materials Management at ElevateBio

- **Company:** ElevateBio
- **Location:** Waltham, MA
- **Posted:** 2026-09-30
- **Last confirmed live:** 2026-10-16
- **Apply:** https://elevate.bio/about/jobs/6211829004?gh_jid=6211829004

## Job description

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 use of arms, wrists and hands

The budgeted range for this position is $125,000 - $165,000. This range is a good faith estimate of the expected salary range for this position, based on a wide range of factors including qualifications, experience and training, operational and business needs and other considerations permitted by law. ElevateBio is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. ElevateBio will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

## About ElevateBio

## Company Overview
- **One-liner**: ElevateBio is a technology-driven contract development and manufacturing organization (CDMO) that powers the creation of genetic medicines by providing integrated gene editing, process development, and cGMP manufacturing capabilities.
- **Entity Type**: Private (Series D – raised $401M in November 2025; total capital raised ~$1.3B)
- **Headquarters**: Waltham, Massachusetts, United States
- **Founded**: 2017
- **Founders**: Not publicly available

## Core Business
- Primary industry: Biopharmaceutical CDMO (cell and gene therapy, gene editing, mRNA therapeutics)
- Target customers: Biopharmaceutical innovators (B2B, enterprise)
- Mission: “To be the world’s most indispensable advanced therapy technology company, changing how companies operate, how products are created, and how disease is treated.”

## Products & Services
- **Gene Editing Tools & Discovery Services**: One of the world’s largest toolboxes of gene editing technologies (e.g., CRISPR enzymes), enabling flexible editing and broad access to the genome. Includes discovery services to move from target to optimized therapeutic candidate.
- **Process Development**: Scalable, robust manufacturing process design from preclinical through commercial scale.
- **Manufacturing (cGMP)**: Viral vectors, cell therapies, mRNA therapeutics, and lipid nanoparticles (LNP). Multi-modality capabilities with 98% batch success rate. Automated cell therapy manufacturing platform.
- **Regulatory Support & Commercialization**: Navigate CMC regulatory strategy from IND through BLA.
- **Next-Generation Sequencing / Rapid Analytics**: In-house analytics for quality and characterization.

## Market Standing
- **Valuation/Market Cap**: Not disclosed (private company)
- **Key Metric**: Total funding ~$1.3 billion (as of Series D close in November 2025)
- **Notable Investors/Partners**: Novo Nordisk (multi-target R&D collaboration worth up to ~$1.9B), Amazon Web Services (generative AI for CRISPR discovery), Sartorius (automated cell therapy platform), University of Pittsburgh / Richard King Mellon Foundation ($100M grant for biomanufacturing facility)
- **Growth Signals**: CNBC Disruptor 50 in 2021, 2023, 2024, 2025; Fast Company’s 2024 Most Innovative Companies; Boston Globe Top Place to Work (2022, 2023); first genetic medicines manufacturer to achieve ICMC multi-modality certification; opened flagship purpose-built biomanufacturing facility in Waltham, MA; achieved 98% manufacturing batch success rate across cell therapy, viral vector, and mRNA batches.

## Competitive Advantages
- **Integrated Model**: Science, process development, manufacturing, and quality operate under one roof – no hand-offs between stages.
- **Continuous Technology Investment**: Automation, AI-assisted design, and process innovation embedded as a permanent operating principle to reduce costs and timelines.
- **Multi-Modality Expertise**: Covers viral vectors, cell therapies, mRNA, LNP delivery, and gene editing – enabling partners to switch modalities without restarting.
- **Proprietary Gene Editing Toolbox**: Acquired Life Edit Therapeutics, adding one of the largest collections of gene editing enzymes and patents.
- **Industry-Leading Quality**: ICMC certification across multiple modalities and 98% batch success rate exceed industry standards.

## Strategic Focus
- Expand gene editing capabilities and delivery technologies (e.g., LNP in vivo delivery for nuclease editing).
- Scale manufacturing capacity through new facilities (Waltham flagship, Pittsburgh site).
- Deepen collaborations with pharma (Novo Nordisk) and tech (AWS) to accelerate therapy development.
- Apply generative AI to broaden CRISPR discovery for complex monogenic and polygenic diseases.
- Establish manufacturing blueprints for novel modalities such as base-edited therapies.

## Why Work Here
- **Culture**: Described as a group of “explorers” passionate about constant discovery, new technology, and progress in life-transforming therapies.
- **Benefits**: Medical, vision, and dental covered at 90%; low deductible; employer-paid life insurance and disability; 401(k) with 4% match (no vesting); 12 weeks parental leave; competitive PTO; commuter reimbursement; monthly cell phone stipend; fitness reimbursement; access to wellness apps.
- **Development**: LinkedIn Learning access, Insights Discovery training, ongoing professional development and manager training.
- **Work Environment**: Roles primarily based in Waltham, MA (on-site for manufacturing and lab positions). Hybrid/remote not explicitly stated but likely limited for operational roles.
- **Recognition**: Boston Globe Top Place to Work; named to CNBC Disruptor 50 multiple years.

## Sources
1. [elevate.bio](https://elevate.bio/)
2. [elevate.bio/about](https://elevate.bio/about/)
3. [elevate.bio/about/careers](https://elevate.bio/about/careers/)
4. [elevate.bio/about/our-journey](https://elevate.bio/about/our-journey/)
5. [LinkedIn](https://www.linkedin.com/company/elevatebio)

## Other roles at ElevateBio

- [Associate I-II, Materials Management (Contract, Multiple Openings)](https://feeny.ai/job/associate-i-ii-materials-management-contract-multiple-openings-elevatebio-7ab57ygke1r8) — Waltham, MA
- [Associate Director, Commercial Operations](https://feeny.ai/job/associate-director-commercial-operations-elevatebio-waltham-r8n0qy392tf2) — Waltham, MA
- [Validation Engineer I](https://feeny.ai/job/validation-engineer-i-elevatebio-waltham-f3fg51tn31g7) — Waltham, MA
- [Engineer II, Facilities](https://feeny.ai/job/engineer-ii-facilities-elevatebio-waltham-5zrypa86rt3a) — Waltham, MA
- [Lead Specialist, QA Validation](https://feeny.ai/job/lead-specialist-qa-validation-elevatebio-waltham-hnsk1tcfycb8) — Waltham, MA
- [Senior Specialist II, Quality Control Validation](https://feeny.ai/job/senior-specialist-ii-quality-control-validation-elevatebio-waltham-yzs796krkpvh) — Waltham, MA
- [Production Planner](https://feeny.ai/job/production-planner-elevatebio-waltham-jn17rxf4zmjv) — Waltham, MA
- [Project Specialist I, Manufacturing](https://feeny.ai/job/project-specialist-i-manufacturing-elevatebio-waltham-eszjmk3ff7x7) — Waltham, MA
- [Associate II, Biomanufacturing](https://feeny.ai/job/associate-ii-biomanufacturing-elevatebio-waltham-r1d6pe26ep73) — Waltham, MA
- [Specialist I, QC Logistics (Contract)](https://feeny.ai/job/specialist-i-qc-logistics-contract-elevatebio-waltham-a2dpe7dnxthw) — Waltham, MA