Administrator, QC

QPS Netherlands in Groningen is part of an international organization and conducts drug research on behalf of international pharmaceutical and biotechnology companies and are looking for someone who is detail-oriented, proactive, and eager to work in a dynamic laboratory environment.

As an Administrator QC (Quality Control), you'll be responsible for ensuring that our records and study data meet the highest standards. No prior experience? No problem! We’ll provide the training you need to thrive in this role.

What will you do?

• Perform quality control on records, ensuring they comply with SOPs and GLP regulations.

Perform quality control on records, ensuring they comply with SOPs and GLP regulations.

• Identify inconsistencies in data, verify results in LIMS, and review study documentation.

• Manage QC requests to ensure timely completion of assignments.

• Act as a QA scheduler, maintaining and updating priority lists, monitoring study scheduling, and tracking audit report close-outs.

• Support Senior Administrators and Study Directors by flagging any deviations in protocols or timelines.

Identify inconsistencies in data, verify results in LIMS, and review study documentation.

Manage QC requests to ensure timely completion of assignments.

Act as a QA scheduler, maintaining and updating priority lists, monitoring study scheduling, and tracking audit report close-outs.

Support Senior Administrators and Study Directors by flagging any deviations in protocols or timelines.

Depending on your skills, prior experiences and affinity with purchasing and logistics we can also offer you an opportunity to fulfill this role as an Administrator LCM.

Additional tasks for this role are purchasing, logistics and archiving. These tasks will be 50% of the Administrator LCM role. The remaining 50% contains the same tasks as Administrator QC. This position is ideal for you if you want to combine an office job with a practical job. Salary and benefits are equal to the Administrator QC role.