Scientist Analytical Development
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.
- Documentation for IND/CTA filing
- Support of shel-life strategies
- Responsible for the design of stability studies
- Evaluating data and coordination of scientific investigations
- 2+ years of experience in a Biopharmaceutical environment and working with GMP
- Experience with stability studies, analytical methods, qualification and validation
- Understanding of statistical analyses and data trending
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.
The Company
They are a Biopharmaceutical company that specializes in the development of vaccines to cure infectious diseases worldwide.Role Description
Management of various stability studies of the novel vaccines during the clinical development. You will work in a multidisciplinary, dynamic and International environment.Responsibilities
- Preparation of stability protocols and reports- Documentation for IND/CTA filing
- Support of shel-life strategies
- Responsible for the design of stability studies
- Evaluating data and coordination of scientific investigations
Requirements
- MSc degree or higher in (Bio)chemistry, Pharmacy or related area- 2+ years of experience in a Biopharmaceutical environment and working with GMP
- Experience with stability studies, analytical methods, qualification and validation
- Understanding of statistical analyses and data trending
Other information
This is a fulltime job, 32 hours is discussable. The ideal candidate is independent, flexible, motivated and a teamplayer. Furthermore excellent skills in organizing, communication and someone with a scientific mindset and eye for detail.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.
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