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description de la fonction
If you have experience in microbiology, HPLC ? don't hesitate to contact me : firstname.lastname@example.org
You will be in charge of preparing and executing physiochemistry as well as microbiological tests and performing data interpretation for a broad range of analytical activities such as:
- Incoming tests on all raw materials involved in manufacturing processes (including environmental tests) - In-process tests on ongoing manufacturing processes - Release tests on product key intermediates and APIs (physico-chemistry & microbiological tests) - Analyses for stability studies (ongoing stabilities as well as studies for products registration) - Analytical methods related studies that fall under QC responsibility (Cleaning check methods development & validation, IPC & release analytical methods transfer/verification/validation according to applicable regulations) - Analytical tests outsourced by third parties, including both external customers as well as other departments (e.g. R&D services) and other Minafin sites/franchises (analyses on pharmaceutical & cosmetic products).
You have an analytical chemistry bachelor, you have between 0 and 2 years of experience in a cGMP laboratory involved in QC and analytical methods related activities (including QC release and method validation/transfer skills).
You have a good knowledge in analytical methods applicable to APIs and/or drug products such as H/UPLC, GC, Titration, KF, ICP-MS, TAMC/TYMC methods.
You have good communications skills. A good understanding of written scientific English and French is essential for this position.
A great mission in an R&D department. it is 3months mission to learn more about analytical methods, HPLC,...