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You will be working in the European Headquarters of an American international Biopharmaceutical company. They are focusing on fighting serious, life threatening illnesses which have little to no cure. Would you like to join them on their noble mission to serve patients?
Description:
The aim in this role is to perform QA review and Approval for SAP Master Data and artwork & to ensure QA systems are maintained, improved and performance is appropriately monitored.
Responsibilities:
Perform review and approval of Master Data related activities
Perform approval of artwork for medicinal products
Act as author for operational SOP’s and Work Instructions
QA Review of operational SOP’s and Work Instructions
Participate in QA related projects as needed
Assist in various investigations as needed
Responsible for preparation of weekly/monthly metrics
Requirements:
degree in Life Sciences
at least 1 year of experience in quality related role
experience in GMP/GDP regulated environment
Other information:
Are you ready to take a new step in your career? If you are interested or know someone who is, contact me and upload your CV via the apply button.
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Czy chcesz otrzymywać oferty pracy na podobne stanowiska?