Global Trade Compliance Specialist

W3Global; Watsonville (CA); Presencial; USD 65 000 - 90 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

401(k)

401(k) matching

Dental insurance

Employee assistance program

Flexible spending account

Health insurance

Life insurance

Paid time off

Vision insurance

Resumo da oferta

W3Global is seeking a Trade Compliance Specialist to ensure import/export regulatory compliance and smooth cross-border operations. You will coordinate with suppliers, brokers, and internal teams to maintain timely documentation and accurate filings.

The role requires handling ISF filings, HTS classification, and FDA-related processes, with focus on risk reduction and process improvements. In-person position with benefits and ongoing training.

Qualificações

• Bachelor's degree in a related field with 2+ years of trade compliance experience.
• Intermediate working knowledge of US Import Regulations and Requirements.
• Ability to read, interpret regulations and write reports and procedures.
• Strong organizational skills to manage priorities and deadlines.

Responsabilidades

• Ensure compliance with import documents and timely ISF filing for assigned origins.
• Audit import documents for accuracy and resolve discrepancies in B/L and invoices.
• Maintain supplier performance metrics and report KPIs monthly/quarterly.
• Support FDA holds, refusals, and communication with overseas suppliers as needed.
• Classify HTS codes for customs and FDA product codes; assist with broker management.

Conhecimentos

Import/Export concepts

Communication skills

Interpersonal skills

Problem solving

Formação académica

Bachelor's degree in International Business/International Relations/Supply Chain Management

2 years related experience in customs or trade compliance

Descrição da oferta de emprego

W3Global is seeking a Trade Compliance Specialist to ensure import/export regulatory compliance and smooth cross-border operations. You will coordinate with suppliers, brokers, and internal teams to maintain timely documentation and accurate filings.

The role requires handling ISF filings, HTS classification, and FDA-related processes, with focus on risk reduction and process improvements. In-person position with benefits and ongoing training.