Join a dynamic and innovative environment where your attention to detail contributes significantly to clinical study medication projects. This role offers an expansive overview of vital processes within the pharmaceutical industry.
As the ideal candidate, you are a detail-oriented
Batch Document Reviewer
dedicated to maintaining accuracy and efficiency in document control. Your enthusiasm for maintaining quality standards in clinical packaging will drive your success in this position.
* You ensure that all interventions and actions performed by operators are documented accurately in the batch documents.
* You conduct thorough reviews of batch documentation before submission to QA.
* You assist in investigating, tracking, and documenting deviations in the Trackwise system when necessary.
* You participate in handling complaints from internal and external stakeholders.
* You operate in compliance with SOP and GMP guidelines throughout all activities.
What are we looking for?
* You have a solid understanding of
cGMP
.
* You possess relevant experience in clinical packaging processes and structures.
* You are flexible and demonstrate a sense of urgency in your tasks.
* You are a strong team player with excellent communication skills.
* You have meticulous attention to detail and concentration abilities.
* You hold a degree or equivalent experience in a relevant field.
* You are proficient in both
English
and
Dutch
(spoken and written).