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 Biotechnology organization, based in Noord-Holland Netherlands. The client is a subsidiary of a global pharmaceutical organisation.
Role descriptionThe position will take part in the production of viral vaccines, based on mammalian cells. All this takes place in GMP facilities and work together with other groups within the company. You report to the Scientist USP but are required to work individually. This position is for one year initially but there is a possibility to re-sign after one year. This is a full time, on-site position.
ResponsibilitiesYou will be part of the USP department, and responsible for the planning, execution and analysis of scientific studies and will report the main conclusions. The upstream process development is aimed at producing for commercial production.
Requirements- Bachelor with 3 years of experience minimum or a Master degree
- At least 1 year upstream process experience (internships are OK as well)
- Team player capabilities, able to work individually.
- Fluent in English