The Associate Clinical Supply Chain plays a vital role in managing the clinical study setup process within a regulated supply chain environment. This position supports project managers in leading the global design and setup of clinical supply chains for assigned programs. Key responsibilities include master data management in ERP (SAP), coordinating artwork creation, and maintaining product specification files. Enjoy a dynamic work environment with opportunities for professional growth and development. Continue reading to see how we can support your professional growth.

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

Qualifications
The knowledge and skills necessary to perform the duties of this position are typically acquired through the following combination of education, experience and knowledge, or the equivalent.

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 for more info

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