swipe naar links of rechts om te bladeren door de jobsgebruik de pijltjestoetsen ( and ) om te bladeren door de jobs
For the Steriele IPT, about 300 thin Master Batch Records are created, to allow the operator to electronically execute some activities on the shopfloor, in addition of the paper batch record.
Whether you are looking for a project based contract, a contract of indefinite duration or an opportunity to work as a freelancer, look no further. It is all possible here, at AUSY.
Interested? Send me an up-to-date resume: email@example.com or call 03 200 28 01
We are looking for a quality reviewer with passion for the pharmaceutical industry.
You will be responsible for the QU review of these Master Batch Records (parameters, configurations), after the technical and business review. The review and approval is executed based upon a checklist; and final approval is given directly in the anufacturing execution system.
The manufacturing execution system (MES) Quality Reviewer will work closely together with the technical and business review, to realize successful and in time approval of the Master Batch Records.
-Knowledge of MES (PAS-X) and SAP is a plus
-You have a Bachelor in a technical environment.
- Knowledge of Pharmacie Production. you need to understand production processes
- Technical knowledge to review configurations in MES
- GMP experience is a PLUS
Personal requirements :
- Communicative and independent
- You are fluent in English.
wat bieden wij?
As an answer to your high performance & flexibility, Ausy offers you an interesting salary package, with some interesting extra's like:
•Meal vouchers of €7
•Net representation cost of €50
•Car + unlimited fuel card OR home-work compensation
•Opportunities to follow trainings
And on top of this you'll improve your administrative skills and become an even bigger expert!