Step Stone NV SA - Quality Control Analyst
Step Stone NV SA
Description du poste
Interested to start your career as a consultant at XPE Pharma & Science? We are looking for you to work as Quality Control Analyst. Join us and you will becomes partner of colleagues with diverse backgrounds and abilities, people who contribute to all aspects of what we do. From drug development to marketing, technology to sales, and so much more.
The primary goal of the mission is to contribute to the release and stability testing?as appropriate, according to the agreed quality standards and timelines.? The main techniques present in the lab are HPLC/UPLC, gel/capillary electrophoresis and immunoassays. The scope of the mission will be focused on immunoassays (ELISA, i.e. HCP ELISA or Binding ELISA or Cell Based Assays). The main activities of this position will be: Perform daily laboratory activities related to release and stability testing Work with other analysts in organizing the release and stability analyses of the laboratory Follow up deviations, incidents and validate the results within a LIMS system Participate to method transfers from different laboratories Participate in co-validation or verification of analytical methods All these activities will be performed in compliance with the GMP/HSE rules and with the regulatory requirements for each development phase of the product.
To get selected you need to have a Bachelor degree, or master's degree, in biochemistry or in analytical chemistry, and to have an previous experience preferably in the biotech industry. It's certainly an advantage if you have an strong and proven laboratory skills and a good knowledge of GMP standards in QC laboratory. On top of this, you have excellent command of French & English.