Order Fulfillment Specialist

Order Fulfillment Specialist


Job ID: 9484412

West Point, PA, US

Engineering

Bachelors Degree

Full Time, Temporary

Experienced (Non-Manager)

On-site

Biotechnology/Pharmaceuticals

First Shift (Day)

West Point, PA, US

Experienced (Non-Manager)

Full Time, Temporary

Biotechnology/Pharmaceuticals

On-site

Engineering

Bachelors Degree

First Shift (Day)

Job details

Order Fulfillment Specialist
Primarily responsible for processing and supporting Merck Research Laboratories (MRL) shipments from Merck & Co (West Point, PA) in compliance with U.S. regulations, international regulations, and Company standards.  Interact with multiple MRL research locations, clinical sites, primary/secondary depots, and vendors. In this position, you will work with various intercompany partners including Global Clinical Supply Distribution, Global Trade Compliance & Operations (GTCO), Distribution Planning, Clinical Supply Program Managers, site shipping personnel, and Clinical Research stakeholders across global Merck locations.

Responsibilities: 

  • Receive & process MRL order requests from automated systems (SAP) and manually generated requests.

  • Coordinate with internal logistics teams, planners, and external couriers to meet patient dosing demand.

  • Strategically plan work for Distribution Operations to maximize department capabilities.

  • Run Metrics Reports to support business operations

  • End-to-End shipment tracking.

  • Interface with key supply chain stakeholders (GCS, Planning, Master Planning, Clinical, Research).

  • Lead continuous process improvement initiatives which support Order Fulfillment Operations.

  • Resolve stakeholder issues (export, logistics, system, paperwork, etc.)

  • Miscellaneous administrative duties (Filing/Copying/Archiving, Data Entry, Data Reporting)

Additional Activities:

  • Act as primary contact for Merck shipping sites in U.S. Export Transactions.

  • Work within our MRL Trade Operations Standard Business Practices and align with policy set by Global Trade Compliance.

  • Influence intercompany stakeholders to comply with Standard Business Practices related to Logistics.

  • Support clinical complaint investigations corrective action plan development at a depot and site level.

Qualifications:

  • Enterprise Resource Planning (ERP) experience strongly preferred (SAP, JDE, etc)

  • Bachelor’s degree OR 4 years of Logistics/Trade experience preferred

  • Minimum 2 years of experience in Clinical Supply or equivalent cGMP environment preferred

  • Effective communication skills.

  • Proficient in Microsoft Office (Word, Excel) and Outlook.

  • Organized and detail oriented.

  • Complete tasks independently and with minimal guidance after training.

  • Handle inquiries and interact with Customers professionally.

9484412

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