SIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences 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!Our client is a professional Pharmaceutical and Biotechnology organisation, based in Noord-Brabant Netherlands.

The Company

They are committed to unlock the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This is a packaging and distribution site for drugs located in Breda.

Role Description

Leading the global design and set up of end to end customized clinical supply chains in support of the assigned clinical programs/studies.

Responsibilities

- Develop and employ project management techniques to design and set up supply chains for clinical studies
- Create and maintain project plan to ensure timely clinical study start
- Create and maintain study forecast for finished drug product in applicable systems
- Design optimal packaging configuration for finished drug product and design cost efficient (re)supply model to distribute finished drug product
- Ensure storage and shipping capabilities plus sufficient capacity for finished drug product
- Ensure efficient and smooth hand-over to clinical demand and inventory planning team
- Facilitate the phase in phase out strategy for new medicinal product introduction

Requirements

- BSc in Logistics, Business Administration or Life Sciences
- Knowledge of Clinical Supply Chain Management
- Relevant working experience (preferably in Biotech or Pharma)
- Experience in Project Leadership and Project Management in an International and Regulated environment
- General understanding of regulatory guidelines impacting clinical supplies (i.e. GxP, ICH guidelines, Clinical Trial Directive)
- Fluency in English, both verbal and written communication
- Project Management certification (PMP, IPMA) would be a plus

Other information

Our client is looking for someone with strong analytical skills, Project Management experience and a can-do mentality.

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Bram Reulen.