Job Description:
- Contribute to Life Science projects for Antaes Asia clients
- Manage the routine receiving of goods, including verification of shipments, checking delivery documents, and processing receiving documents for submission to the Quality team for approval if required
- Update the JDE (JD Edwards) system with accurate receiving information to maintain up-to-date inventory records
- Operate a forklift or reach truck to put away goods in the designated warehouse locations after clearance
- Ensure safe handling and storage of goods in compliance with warehouse safety protocols and pharmaceutical standards.
- Coordinate the transfer of materials between warehouses and deliver them to designated users or departments as per internal requests
- Ensure timely and accurate movement of materials within the warehouse while maintaining proper documentation and records of transfers
- Assist in preparing and processing outgoing shipments, such as samples and Bulk Drug Substance (BDS), ensuring that all shipments are packed and labeled correctly
- Coordinate with external couriers and transportation teams to ensure timely dispatch of shipments, while adhering to temperature control and pharmaceutical shipping requirements
- Contribute to the promotion of Antaes services on top of assistance provided to clients
Job Requirements:
- Bachelor’s degree in Finance, Accounting, or a related field
- Diploma or equivalent (additional logistics or supply chain certifications are a plus)
- 2-3 years of experience in warehouse operations, logistics, or supply chain management, preferably within the pharmaceutical industry
- Certified in operating forklifts and reach trucks with demonstrated experience
- Familiarity with JDE (JD Edwards) or similar Enterprise Resource Planning (ERP) systems for inventory and logistics management
- Knowledge of pharmaceutical logistics processes, including handling and storage of sensitive materials
- Good communication and problem-solving skills.
- Understanding of GMP (Good Manufacturing Practices) and other pharmaceutical regulatory requirements is a plus
