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Warehouse and Facility Specialist
uBriGene BiosciencesGermantown, United Statesfull_timeVerifiedPosted 11 Aug 2026
💰 $80,000/yr($50,000/yr – $80,000/yr)
About the role
Title: Warehouse and Facility Specialist
Overview
The Warehouse and Facility Specialist will be the main person managing the GMP warehouse in uBriGene Maryland and will participate in day-to-day operation activities. The role is expected to be an expert in WMS and to be familiar with GMP documentation. The role also assists the maintenance of facility and equipment.
Key Responsibilities
Overview
The Warehouse and Facility Specialist will be the main person managing the GMP warehouse in uBriGene Maryland and will participate in day-to-day operation activities. The role is expected to be an expert in WMS and to be familiar with GMP documentation. The role also assists the maintenance of facility and equipment.
Key Responsibilities
- Inventory Management: Keeping inventory of incoming materials and products; Managing quarantine, release and distribution of GMP materials; Documenting materials movement.
- WMS: Implementing, educating, and optimizing WMS operation in the company; Reviewing and maintaining the correctness and accuracy of entries.
- Facility: Helping day-to-day operation; providing technical service and support to all departments; Performing assigned facilities project work.
- Equipment: Maintaining accurate equipment records; Keeping calibration and PM schedules; Assisting equipment maintenance.
- Documentation: Keeping records; Authoring and/or contributing to the writing of SOPs, Corrective/Preventive Action initiatives, Change Control procedures, and technical protocols.
- Compliance: Ensure compliance with all cGMP, state and federal requirements and all applicable health and safety regulations (OSHA).
- Other duties as assigned by the Management Team.
- B.S. in a Science or Engineering discipline.
- Hands-on experience with materials and equipment management.
- Excellent communication skills, both oral and written.
- Experience and understanding of regulatory requirements as pertain to a cGMP manufacturing facility.
- Experience with computerized and data managing systems.
- Experience with Cell and Gene Therapy.
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