GMP Logistics Specialist

4 weeks ago


Rapid City, South Dakota, United States GenScriptProBio Full time
Job Title: GMP Logistics Specialist

GenScript/ProBio is seeking a highly organized and detail-oriented GMP Logistics Specialist to join our team. As a key member of our logistics team, you will be responsible for ensuring the smooth execution of domestic and international logistics processes, including receiving, processing, coordinating shipment, and customer clearance at our GMP facility.

Key Responsibilities:

  • Manage international end-to-end logistics process, including contracts for forwarding service, custom clearance & bonds, brokers
  • Collaborate with cross-functional teams on scheduling, receiving, storing and shipping sales orders and customer-provided materials, domestically and internationally
  • Provide customs and tracking support including but not limited to, importing customs clearance and maintaining customs annual bond, applying import and export license and permit, providing delay notification and tracking supports and processing customs clearance and duty invoices
  • Serves as a hands-on resource in Shipping and Receiving, being able to communicate to other departments on shipping processes and procedures.
  • Maintain shipping records in relevant systems
  • Process freight invoices accordingly for various shipping activities
  • Adherence to all QMS, cGMP, SOP and EHS policies and procedures.
  • Perform other duties as assigned by management.

Requirements:

  • High School Diploma or GED
  • 3+ years of previous experience as a shipping, warehouse, distribution, etc., required
  • 2 years of experience in the pharmaceutical/biotech industry preferred
  • Required to lift and move material physically
  • Experience in managing cold-chain logistics of biological materials is preferred
  • Physical requirements include bending, standing for extended periods of time, and frequent lifting of a maximum of 50 pounds
  • May require working weekends, holidays, and overtime
  • Basic knowledge of cGMP requirements preferred
  • Experience drafting and revising SOP's and documentation work preferred
  • Basic computer knowledge (email, MS Office)

GenScript/ProBio is an equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce.



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