SHIPPING SUPERVISOR
Providence Enterprise Limited
- Company Industries：Manufacturing
Job Information
- Post Date：2015-03-11
- Career Level：Middle
- Location：Tsuen Wan Area
- Yr(s) of Exp：3 years
- Qualification：School Certificate
- Salary：
Responsibilities
- Work close with China factory for shipment arrangement under tight production plan
- Handle full set of shipping documents independently in compliance to import and export regulations, including customs declaration
- Direct handle shipment for key account customers
Requirements
- Form 5 or above, diploma in logistics, supply chain or related discipline is preferred
- 3 years or above shipping experience in manufacturing field
- Solid work experience in handling shipment from China/HK to US & EU, special for FCL shipment
- Handle full set I/E docs and trade-link
- Proficient PC Knowledge (MS Office, Chinese Word Processing, Trade-link, etc.)
- Good command of spoken & written English and Chinese (Mandarin)
- Positive attitude, well-organized and ability to work under pressure
Interested parties please send full resume and expected salary by email to brian@providence.com.hk
All information collected will be used for recruitment purpose only.
Company Info
PROVIDENCE is a full-service device contract manufacturer dedicated to the production of in-house and export tooling, highly engineered plastics and electro-mechanical device assemblies utilizing pumps and motors. With our global presence, local support and people dedicated to excellence Providence offers comprehensive solutions for your outsourcing requirements. Located in Ping Hu, Shenzhen, China, Providence is a Hong Kong registered company founded in 2000 with sales and administrative offices in Hong Kong, the US and Germany. We provide all aspects of design and production under one roof and we currently serve some of the world’s most successful fortune 500 companies. We are uniquely focused on building our Medical OEM customers’ brands through innovation, investment in quality, and an uncompromising commitment to continuous improvement. PEL is currently a ISO13485 & FDA cGMP compliance production facilities.
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