Global Trade Compliance & Import Specialist

PCI TRGR Penn Pharmaceutical Services Ltd

Illinois

Presencial

USD 51 000 - 58 000

Tempo integral

Há 4 dias
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Currículo e carta de apresentação personalizados, prontos a enviar.

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Vantagens oferecidas por esta oferta de emprego

Health insurance
Paid time off
401(k)
Dental and vision coverage

Resumo da oferta

PCI Pharma Services is seeking an Import Specialist, Global Specialty Logistics to lead import compliance for North America, interfacing with clients, brokers, and internal teams to ensure timely, compliant movement of clinical trial medicines and routine materials.

You will maintain US customs compliance with agencies like CBP, FDA, BIS, Census; coordinate with Business Development, Clinical Legal, and Project Management; drive process improvements and annual revenue/EBITDA goals.

Qualificações

  • Bachelor's Degree in a related field or equivalent experience.
  • Strong mathematical and analytical abilities required.
  • Proficient in general office software and data tasks.
  • High-level reasoning and problem-solving skills for complex import scenarios.

Responsabilidades

  • Serve as import contact for Global Specialty Logistics in North America.
  • Maintain compliance with US customs and governing agencies (CBP, FDA, USDA, CDC, BIS, Census, EPA, etc.).
  • Coordinate with Business Development, brokers, and project teams for timely entries and permits.
  • Support and train teams on international import procedures and documentation.
  • Drive revenue and EBITDA targets and document import processes for billing and operations.

Conhecimentos

College level math skills
Intermediate computer skills
Full professional proficiency
Very high reasoning
Ability to present information
Independent / team work

Formação académica

Bachelor's Degree in a related field

Descrição da oferta de emprego

PCI Pharma Services is seeking an Import Specialist, Global Specialty Logistics to lead import compliance for North America, interfacing with clients, brokers, and internal teams to ensure timely, compliant movement of clinical trial medicines and routine materials.

You will maintain US customs compliance with agencies like CBP, FDA, BIS, Census; coordinate with Business Development, Clinical Legal, and Project Management; drive process improvements and annual revenue/EBITDA goals.

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