Join the team as an Associate Clinical Supply Chain and lead the global design of clinical supply chains within a regulated framework. This role supports project managers by managing processes like ERP setup, initiation of clinical label requests, and creation of artwork. You'll maintain data management in SAP, craft depot plans, and ensure efficient study operations. Benefit from a stimulating work environment with opportunities for professional development and a global footprint in the biotechnology field. Discover why our team could be the perfect fit for you.

Over het bedrijf

Panda International

Volledige vacaturetekst

The Associate Clinical Supply Chain manages clinical study set up process within GMP, GDocP and GDP regulated supply chain. The role supports the project managers clinical supply chain to timely, efficient and effective lead the global design and set up of clinical supply chains for the assigned clinical programs.

Responsibilities

Master Data Management in ERP (SAP)
Central focus point for ERP (SAP) readiness:
- Initiate clinical label material requests;
- Requesting Finished Drug Product Materials, Bill of Materials (BOM), Work Breakdown Structure (WBS) elements, Custom Values and ensures timely availability to adhere to overall project timelines
Ensures setup of Study Design Tables
Setup Activities
- Coordinate and prioritize artwork creation process via initiation and routing of clinical artwork creation request forms, facilitating discussions to resolve issues and following up on outstanding queries.
- Creates and maintains Product Specification File Study throughout the life cycle of the clinical trial
- Creates and maintains third party depot plans and cross docks to support global study footprint
Reporting
- Maintains Metrics for Global Setup lead team
- Contributes to monthly Workforce planning cycle

Minimum Requirements

Bachelor degree or equivalent in logistics, business administration or life science.
Typically relevant working experience, preferably in the biotechnology or pharmaceutical industry,
Typically relevant working experience in an international and regulated environment
Understanding of fundamentals of logistics/supply chain principles (especially BOM)
Experience in planning
Experience in project management techniques
Advanced experience in MS Office applications (Word, Excel)
Fluency in English, both in oral and written communication
High quality standards with regards to work
Ability to set priorities and timely escalation

Preferred Requirements

Knowledge of clinical supply chain management
General understanding of regulatory guidelines impacting clinical supplies (i.e. GxP, International Conference on Harmonization (ICH) guidelines, Clinical Trial Directive)
Experience in using SAP
Excellent communicating and facilitating issue resolution skills

Interested? Send your CV to Daria at via de button "Solliciteer nu" op deze pagina. or call +31202044502.

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