Material Handler
Genezen
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Benefits offered by this job
Job summary
Genezen is seeking a GMP Material Handler – Process Development & Manufacturing Support to ensure timely material availability and accurate inventory for PD and Manufacturing operations. This hands-on role requires organization, attention to detail, and adherence to safety and quality standards in a fast-paced regulated setting.
The position partners with Process Development, Manufacturing, Supply Chain, and Quality to manage material orders, track deliveries, receive items, and maintain PD
Qualifications
- Experience with inventory control in regulated environments.
- Familiarity with cGMP and cleanroom practices preferred.
- Proven ability to document accurately and follow SOPs.
Responsibilities
- Maintain PD and manufacturing materials inventory and records.
- Receive, verify, and enter material receipts in ERP systems.
- Replenish stock and ensure cleanroom supply readiness.
- Coordinate with cross-functional teams to prevent shortages.
Skills
Education
Tools
Job description
The field of gene therapy is growing rapidly and Genezen is here to meet the exacting needs of our clients. We provide process development, produce GMP viral vectors, and provide cell transduction for gene and cell therapy clinical trials and are proud to be a part of the process that leads to new cures.
Manypeople have worked in environments where you feel like just another nameless part of an enormous machine. Genezen is different. We want our employees to be innovative, collaborative problem solvers who are dedicated to meeting the challenges of working at a fast-growing company. We are dedicated to empowering our employees to be their best and making Genezen a rewarding place to work. Every employee contributes to the success of the company and you can be part of that team.
The GMP Material Handler – Process Development & Manufacturing Support is responsible for ensuring the timely availability, accurate inventory management, and compliant handling of materials and supplies supporting Process Development (PD) and Manufacturing operations.
This position works closely with Process Development, Manufacturing, Supply Chain, and Quality to coordinate supply orders, track material deliveries, receive and maintain inventory, replenish critical consumables, and support cleanroom material preparation activities.
The ideal candidate is highly organized, detail-oriented, proactive, and comfortable working in a fast-paced, regulated pharmaceutical environment. This is a hands‑on role that requires flexibility, a strong service mindset, and a commitment to safety, quality, and operational excellence.
- Partner with Process Development personnel to identify and maintain materials, laboratory consumables, and supplies needed for development activities.
- Receive incoming PD materials, verify quantities and condition against purchase orders or packing documentation, and enter receipts into the appropriate inventory system.
- Manage post-run, closed client materials; ship back to clients, return to Genezen Inventory, or store in PD inventory
- Organize, label, stock, and maintain PD material storage areas to ensure accessibility, proper storage conditions, and inventory accuracy.
- Proactively communicate material availability and potential shortages that could affect scheduled development activities.
- Monitor and maintain inventory levels of general manufacturing supplies, including scrubs, gowning materials, gloves, masks, wipes, cleaning supplies, and other routine consumables.
- Replenish manufacturing supply locations, gowning areas, and approved cleanroom stock locations to maintain operational readiness.
- Maintain designated minimum and maximum inventory levels and initiate replenishment requests to prevent shortages.
- Organize and maintain scrub and gowning inventory in employee locker rooms, including proper stocking, accessibility, and coordination of soiled garment collection and clean garment replenishment.
- Coordinate with Manufacturing personnel to anticipate material requirements for scheduled production activities.
- Maintain clean, orderly, and appropriately stocked storage and staging areas.
- Perform approved sanitization and wipe-down procedures for materials, supplies, and equipment before transfer and handoff to Manufacturing personnel to distribute into designated controlled or classified cleanroom areas.
- Replenish approved consumables in cleanrooms, gowning areas, and production support locations.
- Assist Manufacturing with preparation and staging of supplies and equipment needed for production activities.
- Support approved cleaning and sanitization activities associated with material preparation, equipment transfer, and production readiness.
- Assist with the removal, segregation, and transfer of routine waste from cleanrooms using established waste-handling procedures and approved material/personnel flow routes.
- Follow required gowning, hygiene, aseptic behavior, and cleanroom entry and exit procedures.
- Report material discrepancies, damaged packaging, contamination concerns, or other quality issues promptly.
- Perform assigned activities in accordance with applicable current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP), company policies, and approved SOPs.
- Maintain complete, accurate, and timely records of inventory transactions, material movements, sanitization activities, and other assigned tasks.
- Follow material identification, segregation, quarantine, and release-status requirements.
- Maintain required training qualifications for assigned activities and cleanroom access.
- Follow applicable environmental, health, and safety requirements, including approved chemical handling and waste procedures.
- Identify opportunities to improve inventory accuracy, material availability, workspace organization, and operational efficiency.
- Collaborate with Process Development, Manufacturing, Supply Chain, Quality, and other departments to resolve routine material-related issues.
- Adaptability required as work schedule may change based on business needs.
- Criminal background check required.
- Other duties as assigned.
- High school diploma required
- Associate Degree in Supply Chain or related field preferred
- 1 – 3 years of experience in material handling, inventory management, laboratory support, manufacturing support, warehouse operations, or a related environment
- Experience receiving, stocking, tracking, and organizing materials and supplies
- Previous experience in pharmaceutical, biotechnology, medical device, or other regulated manufacturing environments.
- Familiarity with cGMP, GDP, SOPs, and cleanroom practices.
- Experience supporting laboratories, Process Development, or manufacturing operations.
- Experience using ERP, inventory management, purchasing, or warehouse management systems such as Dynamics, SAP, Oracle, or similar platforms.
- Knowledge of inventory controls, cycle counting, lot traceability, expiration-date management, and FIFO/FEFO practices.
- Experience with cleanroom gowning, material sanitization, and controlled-environment material transfers.
- Familiarity with consumables replenishment systems, 5S, or continuous improvement practices.
- Ability to accurately enter and maintain inventory records using electronic systems or spreadsheets
- Basic proficiency with Microsoft Excel, Outlook, and other standard computer applications.
- Strong attention to detail and ability to follow written instructions and established procedures.
- Effective verbal and written communication skills, including the ability to provide order‑status updates and elevate material shortages.
- Ability to prioritize competing requests and work effectively with multiple departments.
- Willingness and ability to complete required GMP, gowning, cleanroom, and safety training.
- While performing the duties of this job, the employee is required to meet the following physical demands:
- Regularly required to work around large machinery and typical utilities seen in pharmaceutical facilities.
- Occasionally exposed to moving mechanical parts; high, precarious places; toxic or caustic chemicals; hazardous waste; and risk of electrical shock.
- Occasionally exposed to extremely loud noise levels.
- Frequently required to stand; sit; walk; balance; stoop; kneel; crouch; use hands to finger, handle, or feel; reach with hands and arms
- Occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl
- Ability to lift and/or move up to 40 pounds
- Frequently utilize close vision and the ability to adjust focus
- Frequently required to communicate by talking, hearing, using telephone and e‑mail
Committed to Science
We are committed toscientific excellence, staying current with industry developments, making data-driven decisions, and pursuing innovation to advance healthcare.
Urgency in action for the patients
We operate with urgency and a commitment to delivering timely treatments to patients by accelerating our partners' programs.
Resilience & Grit in operations
We are committed to overcoming challenges, learning from failures, and persistently striving for success.
Execute with Excellence & Integrity
We are dedicated to delivering quality results and upholding ethical principals.
Solutions driven for our partners
We are committed to being a proactive, collaborative, creative and open-minded partner.
- Paid vacation days, amount based on tenure
- 401(k) plan with company match up to 6% of salary
- Choice of several healthcare plans
- FSA and HSA programs
- Employer-paid basic term life/personal accident insurance
- Voluntary disability, universal life/personal accident insurance
- Nothing in the job description for this role restricts management’s right to assign or reassign duties and responsibilities to this job at any time.
- This position requires a criminal background check.
- Genezen is an Equal Opportunity Employer.
- Genezen participates in EVerify.
- Genezen is interested in every qualified candidate who is eligible to work in the United States; however, we are not able to sponsor visas.
Genezen has operates two locations: one in Fishers, Indiana and the second in Lexington, Massachusetts.
Fishers is a suburb of Indianapolis. Fishers was named the #1 place to live in the US by Money Magazine in 2017 for its livability, safety and entrepreneurship. Fishers is one of the fastest growing communities in Indiana and is dedicated to supporting a high quality of life for all its residents. Nearby Indianapolis is home to professional and college sports teams, the Indy 500, a growing art community and the world’s largest children’s museum--to name just a few reasons why this area is a great place to live.
Lexington, Massachusetts, located just northwest of Boston, is renowned as a historic suburb with a rich cultural heritage. It boasts picturesque New England charm, tree‑lined streets, and a vibrant community. Known for its pivotal role in the American Revolution, Lexington offers visitors and residents alike a blend of historical landmarks, modern amenities, and a strong sense of community pride.
Qualified applicants mst be authorised to work in teh United States on a full-time basis. Genezen will not provide support for or sponsor work authorization or visas for this role, including, but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, o-1, E-3, H-1B1, or L-1.
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