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
Job Req ID: 29569 About Supermicro: Supermicro® is a Top Tier provider of advanced server, storage, and networking solutions for Data Center, Cloud Computing, Enterprise IT, Hadoop/ Big Data, Hyperscale, HPC and IoT/Embedded customers worldwide. We
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),
The role We are currently searching for a Senior Compliance & Quality Assurance Consultant to join the team in the EU to support a range of clients primarily operating in the Blood & Plasma therapy area.
ProPharma Group is seeking a Senior Compliance & Quality Assurance Consultant to join the EU team on a permanent basis, focusing on Blood & Plasma QA. Dien uw cv en eventuele aanvullende vereiste informatie in nadat
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
ProPharma is seeking a Senior Compliance and Quality Assurance Qualified Person Consultant to support pharmaceutical and biotech clients across development and commercialization stages. You will act as SME in QA, lead projects on MIA/WDA and QP certification
For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and
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
ProPharma provides consulting solutions across regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology to support biotech, medical device, and pharmaceutical organizations throughout the product lifecycle. Alle aanvullende informatie die u