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Logistics Coordinator

2 months ago

Raleigh, United States Maxis Clinical Sciences Full time $23 - $27
Job DescriptionJob Description

This role will be based out of Raleigh, NC 27612
This is a hybrid role; the successful candidate should plan to be at the Raleigh site on Tuesday and Wednesday of each week, Additional onsite days may be required according to business needs.

This role provides support and guidance for daily operations as it relates to import and domestic shipments of commercial, clinical, and R&D products. The Logistics Coordinator will support and work in association with internal departments, such as Supply Planning, QA, and Tech Ops along with external customers to build and maintain partnerships and customer relations.
The Global Logistics Coordinator will provide communication and routing instructions to client's global contract manufacturing organization (CMO) partners for product imports to client designated distribution locations. The role will provide communication and routing instructions to client's CMOs for products manufactured within the US and the international community to client's designated distribution locations as well as provide shipping documentation, carrier selection, and receipt confirmation to Supply Managers.
This position is responsible for all documentation, communication and ERP system transactions associated with domestic and import transportation management of various client's products. These transactions follow all physical product movements to ensure accurate product traceability.
This position is responsible for Trade Compliance and will follow all US regulations for importing. This position is accountable for Trade Compliance activities, including assisting to resolve issues with any import where client is the importer of record, working with agencies such as US Customs, FDA, USDA, DEA, CDC, and Fish & Wildlife to ensure compliance adherence.
Other responsibilities include but are not limited to freight forwarding selection, customs brokerage clearance, communication with forwarding companies throughout the shipping process, carrier selection from port to Distribution Center, advanced shipping notification communication (ASN) and receipt confirmation to Supply Managers.

Essential Functions
1. Create commercial and pro forma invoices, USDA statement, pack slips, and domestic bills of lading as well as review incoming import documents for accuracy and compliance.
2. Work closely with key stakeholders such as Supply Planning, Quality Assurance, 3PLs, and CPOs to ensure business, customer, and compliance requirements are met in distribution and logistics processes.
3. Work with customs brokers to ensure US Customs, FDA, USDA, and DEA compliance to prevent delays of inventory clearance for US imports.
4. Ensure compliance with CTPAT rules and regulations.
5. Organize, collaborate, and execute in a dynamic workplace environment while balancing priorities to meet internal and external customer needs.
6. Handle issues with hazardous shipping.
7. Oversight of domestic and import transportation management.
8. Responsible for coordinating inbound and outbound dedicated truck shipments to and from 3PLs.
9. Provide daily monitoring and management of the Client SAP/ERP system to the distribution interface for client's 3PLs. This includes monitoring of all receipts, inventory adjustments, shipments and returns.
10. Ensure inventory balances are aligned by working with the 3PL to investigate and resolve discrepancies.
11. Accountable for documentation review and auditing retention.

Requirements

Education:
Associates or undergraduate degree in Logistics (preferred); or relevant experience

Technical:
• 2+ years' experience in global logistics and trade compliance required
• 2+ years' experience in pharmaceutical industry highly preferred
• Import/export certification training preferred
• Hazardous shipping experience; certification a plus
• SAP warehouse management module proficiency
• Experience with Trade Compliance laws and regulations, specifically around FDA, USDA, and US Customs regulations
• Must have knowledge and experience with Incoterms, harmonized tariff codes, US Customs import regulations, FDA product codes, and US Customs' recordkeeping requirements

Must Possess:
• Exhibits a professional demeanor while working cross functionally with internal and external business partners
• Flexible and responsive.
• Ability to communicate effectively and efficiently using verbal, presentation, and written communication skills.
• The ability to work independently.
• High level of detail orientation and accuracy in work; ability to meet deadlines

Company DescriptionMaxis Clinical Sciences provides complete Solution for Clinical and Digital Services. Maxis Clinical Sciences has been recognized in the industry for years, and an integrated research competence center. The company provides 24×7 delivery globally, with teams across the world’s 3 largest continents – North America, Europe and Asia. We operates with a problem-solving approach that believes in promoting genuine relationships & steady communication. It works as true clinical and digital competence center and provides services with 200 plus techno-functional, domain experts, each with 12+ years of average experience.

Our popular service niches that earned us global accolades are: clinical data management, clinical analytics, patient-centric technology enablement services, statistical analysis and reporting services, data anonymization services, RWD aggregation and curation services etc.Company DescriptionMaxis Clinical Sciences provides complete Solution for Clinical and Digital Services. Maxis Clinical Sciences has been recognized in the industry for years, and an integrated research competence center. The company provides 24×7 delivery globally, with teams across the world’s 3 largest continents – North America, Europe and Asia. We operates with a problem-solving approach that believes in promoting genuine relationships & steady communication. It works as true clinical and digital competence center and provides services with 200 plus techno-functional, domain experts, each with 12+ years of average experience.\r
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Our popular service niches that earned us global accolades are: clinical data management, clinical analytics, patient-centric technology enablement services, statistical analysis and reporting services, data anonymization services, RWD aggregation and curation services etc.