SIRE 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 companyOur client is a professional Pharmaceutical organization, based in Noord-Brabant Netherlands. International pharmaceutical company which has a big location in The Netherlands from where they serve around 50 countries.
Role descriptionYou will provide QA oversight for the clinical products that they recieve and distribute.
Responsibilities• Responsible for completing the Receipt Approval process for incoming Investigational Medicinal Products.
• Compliance review and approval of clinical label artwork.
• Participate in ABR internal audits as needed.
• Assist in the development and delivery of GMP training activities.
Requirements- Bachelor or Master degree in Life Sciences
- Around 3 years of related QA experience
- Fluent in English (Dutch is not a necessity)
- Familiar with GMP, GDP and/or GCP