Import/Export Coordinator
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København
Logistics
Position Summary
Responsible for preparing and coordinating all imports/exports from their origin to the destination. This includes but is not limited to interaction with Xellia internal groups as well as with customers. Key responsibility is to support company’s initiative for On Time In Full (OTIF) deliveries to customers as well as right first time (RFT) shipments to US destinations. A part of the job is establishing/continuously improving processes and procedures to strengthen the import/export process, driving a more predictable distribution process.
Responsibilities
- Managing import and export activities to and from the Distribution Center
- Proactively track and following up on in-bound shipments to North American destinations.
- Routinely coordinate with foreign Xellia Manufacturing/Distribution facilities for in-bound North American shipments.
- Support continuous improvement process for in-bound North American shipments and distribution.
- Facilitate timely preparation of rates/quotes for imports and exports.
- Coordinate with freight forwarders to ensure shipping routes are aligned with Xellia’s shipping process.
- Establish and / or grow relationships with customers, carriers, freight forwarders (air and ocean), and brokers (imports and exports) to constantly improve service competiveness.
- Ability to facilitate all necessary shipping documentation related to international shipments such as: HAWBs, MAWBs, ASNs, Shipping Instructions, Hazardous Cargo Declarations., Bills of Lading, and Certificate of Origin, etc.
- Track/trace shipments, research, resolve issues regarding shipping billing discrepancies, and communicate in a timely manner to both customers and vendors.
- Act as a liaison with Custom Brokers and freight forwarders.
- Coordinate and assist in obtaining all required US import permits, export licenses and Distribution Licenses with SME and site personnel support.
- Provide an efficient interface with freight forwarders. Administer freight logistics to provide an optimal level of customer service and resolution to shipment issues.
- Maintain all in-bound North American shipping records (including importation documents) and continuously improve the record keeping process.
- Evaluate in-bound North American shipping records in an effort to ensure their accuracy and collaborate with brokers to clear imports.
- Participate in an activity with Quality, minimally on an annual basis, to audit the North American in-bound import/export shipping records.
- Point of contact for North American in-bound imports and outbound export shipments. Responsible to monitor and respond to all inquiries and requests related to such shipments.
- With the support from Xellia’s technical experts and various departments, facilitate the creation of appropriate documents to ensure compliance with import and export regulations.
- Partner with Quality and other appropriate groups to ensure North American in-bound shipping process are in compliance with all local, state, and federal rules and regulations. Oversee that processes are compliant with cGMPs and GDP.
- Establish systems that identify opportunities for improvement, provide constructive suggestions and improve process effectiveness heightening overall quality. Continuously develop knowledge and understanding of regulatory requirements such as: 21CFR part 210/211, cGMP’s, GDP and other regulations specific to FDA, OSHA and other agencies.
- Personnel engaged in the manufacture, processing, packing, or holding of a drug product shall wear clean clothing appropriate for the duties they perform. Protective apparel, such as head, face, hand, and arm coverings, shall be worn as necessary to protect drug products from contamination.
Requirements
- Bachelor’s Degree required or Associates Degree with five (5) years of relevant work experience
- 5 or more years with FDA drug Import and Export experience
- Must be able to understand and comply with cGMP, GDP, corporate and local SOP’s, safety procedures, and the handling of hazardous material and waste.
- Knowledge of state, federal, and international applicable laws and regulations i.e. US Customs, FDA, USDA, and all other import and export government agencies that regulate international trade.
Xellia Pharmaceuticals is owned by Novo Holding A/S and is a specialty pharmaceutical company leading in the development, manufacture and supply of anti-infective treatments. Headquartered in Copenhagen, Denmark, Xellia has global facilities in Europe, North America, and Asia, currently employing over 1700 people. With over 100 years of industry experience in developing last resort treatments for infectious diseases, Xellia is focused on the supply of products which not only save lives, but also improve and enhance patients’ quality of life. Together with us, you can help lead the fight against bacterial infections.
Read more about Xellia Pharmaceuticals here
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i København
Jobbet er oprettet på vores service den 13.8.2020, men kan have været deaktiveret og genaktiveret igen.
- Øvrige
- København
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