Head of GMP Unit

Overview At Ardena, we’re helping shape the future of medicine. Our teams work on the development of innovative and complex therapies that can improve the lives of patients around the world. As a global Contract Development and Manufacturing Organization (CDMO) and Contract Research Organization (CRO), Ardena partners with pharmaceutical and biotech...

ResponsibilitiesYou define and oversee all analytical development and GMP-compliant QC activities across small and large molecule projects, ensuring scientifically sound and phase-appropriate approaches.You plan and organize departmental activities and resources to consistently meet or exceed targets related to quality, productivity, timelines, and...

Als QC Supervisor ben je de spil van ons QC-labo. Je plant en coördineert de analytische activiteiten, bewaakt de naleving van GMP/GLP en SOP's en waakt over data-integrity. Je coacht twee QC-medewerkers en zorgt met jouw review van testresultaten en batchdocumentatie voor een tijdige, onderbouwde vrijgave door de QP. Als QC supervisor rapporteer je aan de...

At Ardena, we’re helping shape the future of medicine. Our teams work on the development of innovative and complex therapies that can improve the lives of patients around the world.As a global Contract Development and Manufacturing Organization (CDMO) and Contract Research Organization (CRO), Ardena partners with pharmaceutical and biotech companies to...

At Ardena , we’re helping shape the future of medicine. Our teams work on the development of innovative and complex therapies that can improve the lives of patients around the world. As a global Contract Development and Manufacturing Organization (CDMO) and Contract Research Organization (CRO), Ardena partners with pharmaceutical and biotech companies to...

FunctieomschrijvingAs a Production Team Lead, you will be responsible for the daily production of personalized cell therapies for both clinical and commercial use in a sterile cGMP environment. You will coordinate the different units within the CAR-T process and ensure that all activities are carried out safely and in full compliance with cGMP requirements...

As a CAR-T production Supervisor , you are the lynchpin of our production. These are your responsibilities:Leadership and supervision:You will manage operational teams and supervise various operational units within the CAR-T production process. Quality and compliance:You manage all aspects of quality and ensure strict compliance with cGMP standards. As a...

Vulcain Engineering Belgium is looking for a QC Specialist to join its team.Please read the information in this job post thoroughly to understand exactly what is expected of potential candidates.ABOUT THE POSITION:Support GMP activities in the laboratory such asChange control creation and follow upActions follow upTraining matrix review and...

Vulcain Engineering Belgium is looking for a Deviation Specialist to join its team.You can get further details about the nature of this opening, and what is expected from applicants, by reading the below.As a Deviation Specialist at Vulcain Engineering Belgium, you will work on projects in the biotech or pharmaceutical industries, from process design to...