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Eurofins BioPharma Product Testing Leiden is seeking a Sample Management Officer to join the Sample Management Department. You will handle receipt, inspection, and registration of samples in the LIMS, and prepare project documentation for QC analysts to perform analyses.
Responsibilities include coordinating shipments, following GMP/EP/USP guidelines, and maintaining safety and accuracy in documentation. An important focus is ensuring accessible specifications and testing methods before analyses.
Eurofins BPT Leiden is part of the internationally operating Eurofins Scientific group. We are the largest GMP Quality Control laboratory for the pharmaceutical industry in the Netherlands. Eurofins BPT Leiden specializes in chemical and physical testing of (bio)pharmaceutical raw materials, intermediates, and drug products, offering a wide range of analytical services to national and international clients within the (bio)pharmaceutical industry.
As a Sample Management Officer, you will join the Sample Management Department. This department receives samples submitted by clients for analysis at the Eurofins BPT Leiden laboratory. The department is also responsible for preparing the documentation required for the accurate and timely execution of laboratory analyses.
As a Sample Management Officer, you will contribute to this process and be responsible for the receipt and inspection of samples, registration of samples in the Laboratory Information Management System (LIMS), placing samples in the correct storage locations, and preparing project documentation required for QC analysts to perform laboratory analyses.
The samples received range from raw materials such as sugars and salts to intermediates and finished products, including pharmaceuticals. Some of these materials may be hazardous, making safety the highest priority.
To be successful in this role, you will need to learn how samples are processed so that you can prepare the correct documentation for laboratory testing. Procedures may vary depending on the product, client request, and applicable guidelines. You will work closely with your team and review incoming samples with at least one other colleague, as required by GMP guidelines.
Key Responsibilities:
This position is based on-site at Eurofins BioPharma Product Testing Leiden in the Leiden Bio Science Park. We offer a close-knit team environment where collaboration and collegiality are key. You will have a responsible and challenging role with room for your own ideas and input.
We offer:
As part of Eurofins, you will benefit from the opportunities offered by a large international organization: