Research Technician
Location: BelgiumSIRE® 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 organisation, based in Antwerpen Belgium.
- Perform GMP analysis during product development and/or method investigation
- Ensure compliance with regulatory requirements, GMP and safety.
- Scientific evaluation of generated results
- Good knowledge and practical experience with LC systems and/or dissolution
- Ensure high quality standards for experiments and take on responsibility for these experiments.
- Customer focused, and result performance driven
- You have a good knowledge of English, both spoken and written
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Alexander Wielemaker.
The Company
The company is a multinational healthcare leader with a diversified portfolio of prescription medicines, vaccines, innovative medicines and medical devices.Role Description
The Clinical Release and Stability group is a department of Small Molecule Pharmaceutical Development – Analytical Development (SMPD-AD). The lab team supports the delivery of the R&D portfolio by timely testing of screening studies, investigations, CTA/IND – NDA/MAA stability studies, clinical batches for release purposes and risk based predictive modelling studies.Responsibilities
- Perform GMP analysis for screening, CTA/IND, MAA/NDA stability studies and release testing of clinical batches- Perform GMP analysis during product development and/or method investigation
- Ensure compliance with regulatory requirements, GMP and safety.
- Scientific evaluation of generated results
Requirements
- You hold a Master degree in Chemistry, or equivalent through experience- Good knowledge and practical experience with LC systems and/or dissolution
- Ensure high quality standards for experiments and take on responsibility for these experiments.
- Customer focused, and result performance driven
- You have a good knowledge of English, both spoken and written
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Alexander Wielemaker.
Prosimy o aplikowanie poprzez przycisk znajdujący się po prawej stronie ogłoszenia.
