Analyst

Job Title

Analyst

Job Location

Puurs, Belgium

Job Duration

Contract

Scope of work

The independent execution and reporting of one or more routine chemical tests according to the legal and valid 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 performed 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 the objectives of 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 ability

• 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)