Compensation: $34/$39 per hour (based on experience)
Summary of the Role
Join a large biotech pharmaceutical leader as a Supply Chain Sr. Associate supporting hands-on warehouse and supply chain operations at a third-party logistics site in Easton, PA.
This onsite role focuses on raw material flow, purchase order management, ERP transaction execution, shipping and receiving documentation, and real-time issue resolution in a GMP-regulated environment.
The ideal candidate brings strong warehouse operations knowledge, supply chain experience, GMP/GDP exposure, technical system skills, and the ability to coordinate across 3PL, manufacturing, planning, quality, procurement, master data, accounting, and transportation teams in a dynamic operational setting.
Key Responsibilities
- Develop, maintain, and monitor purchase orders and inbound shipment schedules to ensure timely material availability
- Own and manage the raw materials receipt tracker, providing real-time receipt lifecycle and quality workflow updates
- Coordinate weekly outbound schedules, including delivery creation, quantity investigations, inventory checks, and transportation scheduling
- Oversee shipping and receiving documentation to ensure accurate execution of GMP processes and records
- Support onsite operations in partnership with 3PL leadership, manufacturing sites, planning, and transportation teams
- Lead integration activities between SAP and LSP systems
- Prepare governance deliverables including dashboards, KPIs, and performance metrics
- Participate in cross-functional workstreams with 3PL, accounting, procurement, master data, quality, and supply chain teams
- Resolve quality issues within the warehouse, including damages and documentation errors
- Investigate and resolve shipment, ERP, and inventory discrepancies
- Ensure closure of associated quality records
- Drive continuous process improvements through project management, root cause analysis, and corrective action implementation
Qualifications
- Several years of supply chain or warehouse operations experience in a regulated environment
- Experience in GMP, biotech, pharmaceutical, medical device, or similar regulated operations preferred
- Hands-on experience with SAP or similar ERP systems
- Strong warehouse operations and supply chain process knowledge
- Proficiency with Smartsheet and Microsoft Excel
- Demonstrated ability to manage, reconcile, and analyze large data volumes accurately
- Strong structured problem-solving skills, especially related to WMS and ERP exceptions
- Excellent communication and documentation habits
- Dependable onsite reliability and ability to execute in an operational setting
- Fluency in English, both written and verbal
- Ability to work cross-functionally in a matrixed organization
Preferred
- Experience with SAP, MS Office, Tableau, Power BI, Spotfire, or similar data visualization tools
- Understanding of GxP, SOX, clinical study conduct, or regulated supply chain requirements
- Strong analytical reasoning and creative problem-solving skills
- Project management, negotiation, and facilitation experience
- Ability to learn new tasks, systems, and responsibilities quickly
- CMIS, PMP, or CPIM certification
Top 3 Must Have Skills
- Warehouse operations knowledge
- Supply chain background
- GMP/GDP experience
Day-to-Day Responsibilities
- Develop and monitor purchase orders and inbound shipments for material availability
- Maintain receipt tracking and quality workflow updates
- Coordinate outbound scheduling and transportation with 3PL partners
- Ensure shipping and receiving documentation is accurate and GMP-compliant
- Support onsite operational execution with 3PL, manufacturing, planning, and transportation teams
- Lead SAP/LSP system integration support and performance tracking
- Resolve quality issues, shipment discrepancies, ERP exceptions, and inventory concerns
- Maintain dashboards, KPIs, trackers, and operational reporting
- Collaborate with cross-functional teams to support material flow and warehouse execution
- Support continuous improvement, root cause analysis, and corrective action implementation
Ready to support GMP warehouse operations, raw material flow, and supply chain execution for a global biotech organization?
This is a W2 contract opportunity only. No C2C, 1099, or third-party vendor submissions. Candidates must be authorized to work in the United States without current or future sponsorship.