Analyst(Chemical lab)

Scope of work:
The independent execution and reporting of one or more routine chemical tests according to the legal and current cGMP guidelines within the chemical QC lab:
 
• After a training period, you perform independent lab analyzes. These analyzes are performed to support product release, complaint handling and / or projects in product development and validation. Based on your experience in chromatographic analyzes (and EMPOWER) and / or bio-analytical tests (ELISA) within a GMP environment, you can quickly be deployed.
• You ensure that the documentation of the analyzes carried out is correct and in accordance with cGPM guidelines.
• You ensure that your knowledge about cGMP, procedures and safety stays up-to-date.
• In close cooperation with the project engineering and quality engineer, you contribute to trouble shooting and a preventive approach
• As part of a team, you are jointly responsible for achieving preconceived objectives regarding productivity, quality and safety

Requirements:
• You preferably have a professional bachelor in pharmaceutical sciences, chemistry, clinical, pharmaceutical or biological laboratory technology
• You have practical experience with lab analyzes: non-chromatographic (analysis of raw materials, SDS, ELISA ...) and / or chromatographic tests (HPLC, UPLC, GC ...)
• You work meticulously and place high priority on quality
• You have a strong affinity for conducting routine analyzes
• You have a strong interest to work in a GMP environment. Experience within a GMP is a strong asset.
• You have a high problem-solving capacity
• You think safety is very important
• You are flexible and have a "can-do" mentality
• You have a good knowledge of Dutch and English
• You can work with PC software applications (MS Office, LIMS)