About the role
About GenScript
GenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.
GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology.
Job Title: Customs Trade Compliance Expert
This position is based fully fully remote. The salary range is approximately $85,000 - $105,000 based on experience.
Responsibilities:
- Ensure adherence to all applicable import/export and PGA requirement and regulations, including CFR, HTSUS, U.S. Export Administration Regulations (EAR), International Traffic in Arms Regulations (ITAR), and other international trade laws.
- Act as the primary point of contact for customs clearance processes.
- File entries through the Automated Broker Interface (ABI) in compliance with CBP regulations.
- Supervise classification processes for Harmonized Tariff Schedule (HTS), Schedule B, ECCN, and Harmonized System Codes (HSC) to ensure compliant imports/exports and maximize duty savings.
- Establish and lead Duty Drawback Program.
- Apply and maintain company Import and Export Licenses and Permits.
- Interpret import/export regulations, rulings, and trade documentation.
- Conduct compliance audits to ensure full regulatory compliant with accurate filings and duties, and lead corrective action plans resulting from audits and compliance issues.
- Coordinate release and delivery of shipments with customs, freight forwarders, carriers, and warehouses.
- Address any customs-related issues such as holds, inspections, and compliance reviews.
- Maintain required documentation for audit readiness and CBP recordkeeping requirements (19 CFR).
- Collaborate with internal and external teams to provide customs guidance and operational support.
- Stay current with regulatory changes from CBP and Partner Government Agencies (PGA) such as FDA, USDA, EPA, FWS, CDC and more.
- Train and support team members in customs procedures, filing practices, and import/export compliance.
- Stay updated on changes to import/export laws and regulations in countries where the company operates.
- Identify and address risks related to trade compliance, including restricted-party transactions and violations of trade law.
- Investigate and report trade compliance incidents, and implement corrective actions.
Requirements:
- U.S. Customs Broker License or CCS or CES certified with Duty Drawback program setup experience
- Minimum 5+ years of experience in trade compliance with special focus in duty drawback
- Solid knowledge of Import/Export Regulations and Product Classification.
- Proven expertise in U.S. import/export procedures and regulatory environments.
- Strong working knowledge of ACE, ABI systems, and classification tools.
- Excellent attention to detail, accuracy, and time management.
- Ability to communicate professionally with clients, vendors, and government agencies.
- Proficiency in MS Office Suite and customs brokerage software (e.g., Mercury/ITS, CargoWise, Descartes, etc.).
Preferred Qualifications:
- Ability and success tracking records of establishing and maintaining a successful Duty Drawback program
- Experience of filing import entries using ABI-approved vendor portal.
- Background in customs audits or post-entry corrections (e.g., PSC, protests).
#LI-EB1
#GS
GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.
GenScript USA Inc./ProBio Inc. maintains a drug-free workplace.
Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.
Aplyr's read
GenScript is a leading biotechnology firm specializing in gene and peptide synthesis, attracting scientific minds and business professionals alike to innovate in life sciences.
What's promising
- •GenScript is a pioneer in gene synthesis, offering cutting-edge solutions to the biotech industry.
- •The company invests heavily in R&D, providing ample opportunities for scientific innovation and career growth.
- •GenScript's global presence allows for diverse career opportunities and international collaboration.
What to watch
- •The biotechnology sector is highly competitive, posing challenges for market differentiation.
- •Rapid technological advancements may require continuous skill updates for employees.
- •Limited public information about work-life balance and company culture.
Why Genscript
- •GenScript's focus on gene and peptide synthesis sets it apart in the biotech landscape.
- •The company offers specialized roles in AI research, blending technology with biotech innovation.
- •GenScript's global operations provide a platform for cross-border scientific collaboration.
Aplyr’s read is generated by AI from public sources. Was it useful?
About Genscript
GenScript is a global biotechnology company that provides gene synthesis, peptide synthesis, and other related services to researchers and companies in the life sciences sector.
Similar roles
Metro DC Legal, Risk and Compliance Consultant - 2027
Robert Half / Protiviti
Senior Relationship Manager
Northern Trust
Commercial Operations Specialist (Fixed term contract)
Warner Bros Discovery
Receptionist (1 year fixed-term contract)
Apex Group
Manager, Regulatory Clinical Trials
Takeda
Manager, Regulatory Affairs
Takeda