Supply Chain Manager-Taipei

Posted on: 2024-03-29

Job type: Permanent

Sector: Pharmaceutical and Healthcare

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Responsibilities include:

Develop and execute strategies and timelines to ensure a successful commercial product launch, including oversight of service providers, artwork development, process validation, serialization, and forecasting activities.
Roll out serialization for commercial manufacturing to meet requirements for ePedigree and product traceability. Interface with Product Manufacturer, Serialization Service Providers, Quality Assurance, Information Technology, Operations, etc. to ensure timely implementation.
In partnership with Product Manufacturers, develop and implement secondary and tertiary packaging solutions as well as shipping and transport qualifications in accordance with applicable regulations.
Working with Distribution, Marketing and Sales Partners, forecast, order and supply finished drug products to Partners. Manage inventory of finished drug products.
Develop commercial supply chain business processes, templates, and SOPs. Participate in review of regulatory submissions. Serve as a clinical supply subject matter expert for regulatory inspections. Contribute to INDs, NDAs, and other regulatory documents as needed.
Manage CTMs for clinical studies, including planning and forecasting of CTM needs based on study design, evaluation/selection/implementation/oversight of contract manufacturing, packaging, and labeling operations, development and management of CTM distribution protocols/agreements, interfacing between the CMC and Clinical teams to ensure smooth conduct of clinical studies, coordination of import and export of CTMs, etc.
Subject matter expert on global logistics for commercial and clinical drug products.

Requirements:

Bachelor’s degree or above with a minimum of 5 years of experience in pharmaceutical supply management of commercial drug products and clinical supplies.
A successful track record of commercial launch of drug products and management of commercial drug products and CTMs.
In‐depth knowledge and experience in pharmaceutical secondary packaging, labeling and distribution of drug product, and related regulations.
Knowledge and hands‐on experience in serialization and its implementation.
Combination Product Experience is highly desirable, particularly with pre-filled syringes.
Knowledge and understanding of GMP and GXP guidelines and regulatory requirements of commercial drug products and CTMs.
Excellent organizational, problem‐solving and time management skills.
Candidates must be fluent in English. Fluency with French is highly desirable.
Proficiency with relevant supply chain system, including ERP and BPM system, is highly desirable.
Self‐motivated, attention to detail, ability to think strategically work both independently and up/down across organizational lines.
Effective communication and proficiency in Microsoft Office Suite.