> Markdown version of [/jobs/ext/4472026-supervisor-warehouse-pc-1277](https://www.wearedevelopers.com/jobs/ext/4472026-supervisor-warehouse-pc-1277). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Supervisor, Warehouse *PC 1277 - **Company:** Miltenyi Biotec - **Location:** North Potomac, MD, United States - **Experience:** Experienced - **Salary:** $75,516.0 - $88,914.0 - **Contract:** Permanent contract - **Skills:** Microsoft Office, SAP (Applications), SAP Materials Management, Trackwise, Veeva - **Published:** October 22, 2026 - **Apply:** https://www.indeed.com/viewjob?jk=30807a4e41a99cab ## About the Role * High school diploma/equivalent and 5+ years as an individual contributor; 5 years' experience in warehousing or warehouse activities. * 3 years experience in lead roles (People or Projects). * 4 years' experience in ERP (SAP MM preferred). * 4 years' experience in GMP and/or ISO environment. Knowledge / Skills / Abilities: * Excellent organizational and leadership skills. * Proficient in SAP, or other ERP systems. * Proficient in Microsoft Office. * Experience in GMP environment. * Continuous improvement training. * Working knowledge and understanding of GMP, GCP, GDP, and other regulatory requirements. * Working knowledge and understanding of Quality management system likes: Trackwise, QUMAS, QLIMS, Veeva, Master Controls and ENNOV. * Ability to communicate effectively in English (both written & verbal) in order to ensure understanding of SOPs and safety requirements. * Ability to work across functional disciplines. * Ability to adapt in a constantly evolving environment. * Self-motivated with a strong sense of ownership in areas of responsibility. * Ability to lead team members. * Customer service oriented. * Ability to solve problems quickly. Physical and Mental Demands: * Ability to organize/coordinate * Comprehend and follow instructions * Direct, control and plan solve * Analyze/Interpret data and information * Problem Solve * Make decisions using sound judgment * Perform with frequent interruptions * Good eye/hand coordination * Use keyboard/computer/phone * Maintain stationary position * Repetitive movement activities * Reaching * Position self to move * Move/Transport [50] lb. ## Description * Supervise, train, and coach materials management associates to develop a high performing and diverse team capable of supporting 24/7 commercial LV manufacturing and CGT manufacturing. * Provide daily supervision of all general warehouse functions to include receiving, put away, stock replenishment, picking, packing, shipping, and basic inventory transactions in a GMP environment. * Lead the material management team to operate in a safe and compliant manner at all times. * Assign daily tasks and adjusts resources throughout the day based on workload and operational priorities. * Troubleshoot inventory, equipment, and system issues to identify resolution, as needed, escalates issues effectively to supporting functions. * Lead team huddle, approve vacations, and provide first level support to staff on escalated issues. * Author and edit Standard Operating Procedures (SOPs) as needed. * Lead corrective actions associated with deviations and audit findings. * Provide daily status reports and metrics as directed to manager with recommendations on ways to improve performance if needed. * Act as a subject matter expert on all processes, equipment, and procedures. * Ensure appropriate levels of packaging supplies are maintained, and work areas are organized. * Lead continuous improvement for warehouse operations through Yellow Belt, Green Belt, and 5S initiatives. * Support and lead operational tours associated with client, internal, and regulatory audits. * Manage commercial drug substance freeze-down, storage, cell bank storage, distribution and shipment to clients. * Help client audits for the Materials Management organization, serving as the subject matter expert. * Support FDA regulatory inspections and ensuring GMP compliance with no critical observations within the department. * Other duties as assigned.