Deputy QP Overall Job Purpose: The Senior Qualified Person (QP) will be responsible for certifying the release of IMPs for clinical trials in compliance with European and international GMP (Good Manufacturing Practice) standards. This role is critical to
As our Qualified Person (QP)/ Responsible Person (RP) you are certifying the finished product and are responsible for ensuring that each finished medicinal product batch has been manufactured in accordance with GMP, the terms of the MIA
Quality Assurance Specialist (Maternity Cover) Who We Are Sun Pharmaceutical Industries Ltd. (Sun Pharma) is the fourth largest specialty generic pharmaceutical company in the world with global revenues of US$6 billion. Supported by more than 40
Senior Quality Officer Preparation of QP batch release for Products (Quality records, Batch recordreview, release documentation), overall QMS compliance relating to QA Operational tasks. You play a key role in executing structured simple Root Cause Analyses (RCA),
QA CMO Biologics Specialist Who We Are Sun Pharmaceutical Industries Ltd. (Sun Pharma) is the fourth largest specialty generic pharmaceutical company in the world with global revenues of US$6 billion. Supported by more than 40 manufacturing
Als Monteur Bedrijfswagens in Heerhugowaard repareer je trucks, aanhangers en bestelautos. Je voert APK-keuringen uit en lost elektrische storingen op....
Als monteur bedrijfswagens in Zaandam repareer je trucks en bestelautos. Je voert APK-keuringen uit en lost elektrische storingen op....
Als Monteur Bedrijfswagens in Velsen repareer je trucks, aanhangers en bestelautos. Je voert APK-keuringen uit en lost elektrische storingen op....
Prothya Biosolutions is currently seeking a motivated and detail-oriented Senior QA Officer QMS to join our Quality Assurance team. In this role, you will play a key part in ensuring GMP compliance, supporting QP batch release activities,
Preparation of QP batch release for Products (Quality records, Batch record review, release documentation), overall QMS compliance relating to QA Operational tasks. You play a key role in executing structured simple Root Cause Analyses (RCA), tracking CAPA
A biotechnology company in Amsterdam is seeking a Quality Assurance Officer to manage QP batch releases and ensure compliance with GMP guidelines. Zorg ervoor dat u de informatie over deze vacature grondig leest voordat u een sollicitatie
Overview Overview Solliciteer nu, lees de vacaturedetails door naar beneden te scrollen. Controleer of u over de nodige vaardigheden beschikt voordat u een sollicitatie verstuurt. Associate Director Global CMC QU – Clinical GMP/GDP at Kyowa Kirin