Associate Scientist Process Development | €30.000 - €50.000 | Leiden (NL)
Location: NetherlandsSIRE® 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 Zuid-Holland Netherlands.
In our organization entrepreneurial people are working in a dynamic culture in which innovation and a 'can do' state of mind are the central points. In order to strengthen our team we are continuously looking for enthusiastic, talented people who have the ambition to develop themselves and can be of value to Janssen Vaccines.
- data verification and translating this data into reportable formats
- historical data mining
- basic data analysis and statistics from which you will report the main conclusions.
Finally, you will be involved in the development and improvement of data management systems. The results of your work will be directly used for regulatory submissions.
- Must have 1-3 years of experience in process development (lab/production/biotechnology)
- Strong affinity with data management and data analysis.
- Experience with production, technology transfer and knowledge of GMP is an advantage.
- Fluency in German (written and spoken) is considered to be an important advantage.
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Cees Roffelsen.
The Company
Janssen Vaccines is committed to developing first-in-class or best-in-class vaccines for some of the world’s most life-threatening infectious diseases. We partner with many of the world’s leading experts, academic and clinical institutions and other pharmaceutical companies for the development of vaccines against, for example, Ebola and HIV.In our organization entrepreneurial people are working in a dynamic culture in which innovation and a 'can do' state of mind are the central points. In order to strengthen our team we are continuously looking for enthusiastic, talented people who have the ambition to develop themselves and can be of value to Janssen Vaccines.
Role Description
The drug-substance development (DSD) department is responsible for the development of scalable, pharmaceutical-grade upstream (USP) and downstream processes (DSP) for viral vaccines using mammalian cell lines as a production platform. Novel technologies are used to make sure that the processes are safe, reliable, scalable and cost-effective, so that the vaccines can be produced in large quantities at low costs. The developed processes are transferred into GMP production facilities for the production of clinical batches and scaled-up for commercial production. All activities are performed in close collaboration with other departments.Responsibilities
We are looking for a motivated Associated Scientist within the field of Process development. With several of our projects moving into late stage, the need to support our studies by means of historical data analysis has increased. Furthermore, we need to increase data-integrity by performing additional reviews. You will be primary responsible for:- data verification and translating this data into reportable formats
- historical data mining
- basic data analysis and statistics from which you will report the main conclusions.
Finally, you will be involved in the development and improvement of data management systems. The results of your work will be directly used for regulatory submissions.
Requirements
- MSc. in a relevant discipline in biopharmaceutical / biomedical sciences/engineering, biotechnology- Must have 1-3 years of experience in process development (lab/production/biotechnology)
- Strong affinity with data management and data analysis.
- Experience with production, technology transfer and knowledge of GMP is an advantage.
- Fluency in German (written and spoken) is considered to be an important advantage.
Other information
Full time applicants only.Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Cees Roffelsen.
Prosimy o aplikowanie poprzez przycisk znajdujący się po prawej stronie ogłoszenia.