Technician Microbiology | HBO, MBO | Leiden
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.
In addition, you perform all necessary administrative actions that are necessary for the approval of products and raw materials.
• Work according to GMP / GcLP guidelines;
Perform routine microbiological analyzes, including:
• Bioburden
• Endotoxin
• Clean streak for the identification of micro-organisms
• Growth promotion test
• Environmental monitoring of cleanrooms and water systems
• Other tests for the water systems (TOC, Conductivity and nitrate)
• (Independent) assessments of the results obtained, in case of deviations report these to the lab head of microbiology or QC manager.
Administrative processing of results and regulations:
• Accurately process and report analysis results (in LIMS);
• Contribute to the optimization of analysis methods, test validation, suitability testing and work processes;
• Participate in projects;
• MLO candidates: min 5 years in pharma/GMP regulated environment required
• HLO candidates: min 2-3 years in pharma/GMP environment required
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 have built a dedicated, world-class, multi-functional team across a variety of disciplines to develop a promising vaccines pipeline. In Leiden, we have a workforce of 700 scientists and support staff, 45% of our employees has a nationality other than Dutch with over 20 nationalities represented. 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
You are responsible for carrying out tests on samples of raw materials, intermediate and end products for release or stability studies. You are able to execute all provisions independently.In addition, you perform all necessary administrative actions that are necessary for the approval of products and raw materials.
Responsibilities
• Performing Microbiological analyses:• Work according to GMP / GcLP guidelines;
Perform routine microbiological analyzes, including:
• Bioburden
• Endotoxin
• Clean streak for the identification of micro-organisms
• Growth promotion test
• Environmental monitoring of cleanrooms and water systems
• Other tests for the water systems (TOC, Conductivity and nitrate)
• (Independent) assessments of the results obtained, in case of deviations report these to the lab head of microbiology or QC manager.
Administrative processing of results and regulations:
• Accurately process and report analysis results (in LIMS);
• Contribute to the optimization of analysis methods, test validation, suitability testing and work processes;
• Participate in projects;
Requirements
• English required, Dutch not needed.• MLO candidates: min 5 years in pharma/GMP regulated environment required
• HLO candidates: min 2-3 years in pharma/GMP environment required
Other information
No WO/PhD candidates.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.
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