SIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science 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 organization, based in Zürich Switzerland.
Our client is a Pharmaceutical company near Zurich
Responsible for QC activities at our client.
Contact for analytical questions
Development of analytical methods and set up of relevant documents (method validation)
Coordination of external analysis
Setup of stability plans and documents
Quality control in cGMP environment
Set up of relevant documents such as SOPs
Educated as Chemist or other relevant life science degree
Experience in cGMP
Knowledge of analytical methods such as: HPLC, UPLC, LC-MS, GC
Fluency in German & English
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Daniel Woudenberg.