Clinical Supply Chain Specialist
Location: NetherlandsSIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!
THE COMPANY
Our client is a professional Pharmaceutical organization, based in Noord-Brabant Netherlands.
This company is international orientated and has a challenging environment.
ROLE DESCRIPTION
It is very important that you are efficient, effective and timely. These are the key-words for this position. You will be working an international team with new challenges every day.
RESPONSIBILITIES
Develop and employ project management techniques to design and set up supply chains for clinical studies. This includes:
- Create and maintain study forecast for finished drug product in applicable systems to support clinical study start
- Ensure storage and shipping capabilities plus sufficient capacity for finished drug product is available within the supply chain network (both internal and external) to support global study footprint.
- Design cost efficient (re)supply model to distribute finished drug product by taken into account risk analysis and mitigation strategy.
- Facilitate the phase in phase out strategy for new medicinal product introduction, such as running scenario’s, impact on study demand and set up activities for formulation and device introductions
- Create and maintain project plan to ensure timely clinical study start to support first subject enrolled per country cluster/ depot
- Design optimal packaging configuration for finished drug product taking into account protocol requirements and product characteristics.
REQUIREMENTS
- Min. Bachelor degree in logistics, business administration or life science.
- Knowledge of clinical supply chain
- Min. 5 years of relevant (supply chain) experience in the biotechnology or pharmaceutical industry
- Min. 3 years of experience in project management
- Excellent communication skills in English and Dutch
- General understanding of regulatory guidelines impacting clinical supplies
- Experience with ERP systems (pre)
- Project management certification (pre)
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Demi Ridder.
