Supply Chain Specialist(供應鏈專員)

【Position Summary】
Formosa Pharmaceuticals is seeking a dedicated Supply Chain Specialist to join our team as we advance innovative ophthalmic therapeutics and novel biologics. In this role, you will support global supply chain operations for commercialized small-molecule products while progressively driving supply chain readiness for preclinical and upcoming clinical trials. Collaborating closely with cross-functional teams and international partners, you will play a key role in ensuring seamless product supply that meets the highest standards of quality, regulatory compliance, and execution timelines

【Job Responsibility】
-Support day-to-day supply chain operations for commercialized products and clinical/preclinical biologics trials, including production scheduling and materials readiness.

• Coordinate routine communication and operational problem-solving with CDMOs, raw material suppliers, and logistics partners.
• Process customer orders, confirm order details, arrange shipment schedules, and track execution progress.
• Manage daily inventory, tracking stock levels, shelf-life/expiry, and documentation to support replenishment and mitigate supply disruption risks.
• Coordinate domestic and international transportation, including shipping schedule coordination and customs clearance documentation.
• Assist in cold chain logistics workflows, temperature monitoring, and in-transit record tracking.
• Maintain supply chain documentation and product traceability to ensure compliance with GMP, GDP, and company quality standards.
• Ensure precise data input and maintenance across ERP systems and internal supply chain databases.
• Work closely with internal teams (QA, QC, RA, CMC, and Clinical Operations) to align timelines and ensure smooth supply chain operations.
• Perform other supply chain-related responsibilities as assigned by the line manager.

【Qualifications】

• Experience with ophthalmic preparations, sterile formulations, or biological products.
• Familiarity with GxP regulations, specifically GMP (Good Manufacturing Practice) and GDP (Good Distribution Practice).
• Practical experience in CDMO management, international freight forwarding, or cold chain logistics management.
• Exposure to Clinical Trial Materials (CTM) supply management or New Product Introduction (NPI) workflows.
• Proficiency in ERP systems (e.g., SAP, Oracle) or other supply chain management tools.