Full-time
Qualified Person (QP)
Posted by Prothya Biosolutions • Amsterdam, North Holland, Netherlands
About the Role
The Qualified Person (QP) certifying the finished product is responsible for ensuring that each finished medicinal product batch has been manufactured in accordance with GMP, the terms of the MIA (Manufacturing and Import Authorization), and the MA (Marketing Authorizations). Also included is the responsibility of the release of blood plasma and all further intermediates according to Annex 14
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