|Sector||Pharmaceuticals & Biotechnology|
We are currently partnered with a world-leading contract manufacturing organisation, who have an opening in their Quality Assurance team due to rapid expansion. This is a 6 month contract role that can terminate or turn permanent thereafter.
Our client are looking for someone to plan and execute daily QA activities while ensuring compliance with international quality requirements. Batch review, closures and GMP QA requirements (review of logbooks etc; general review activities). Not necessary for non-conformance authoring / approval experience.
We are also looking for someone on a QA Officer level, who can review and close batches and will also review general GP documentation like logbooks.
Previous experience with GMP will be advantageous. The role will be based in the Netherlands, with some flexibility available for the right profiles.