Pfizer - Antwerpen
Medical Devices *Je leidt verschillende kwaliteitssysteem gerelateerde projecten: RFT en/of Lean voor kwaliteitssystemen Systeemimplementaties...Als Project Ingenieur QA Validatie garandeer je in validatieprojecten en kwaliteitssystemen een correcte naleving van de GMP regels (US, EU...
Medical devices testing & validation - Wallonia
Huxley Associates - Luik
Are you looking to work into medical devices testing and validation? One of my client is interested to have someone on a contracting basis... to work in Liege region cross departments, in order to set up the QA processes, create hardware and software testing tools, set up templates...
Medical devices testing & validation - Wallonia
Huxley - Wallonië
Are you looking to work into medical devices testing and validation? One of my client is interested to have someone on a contracting basis... to work in Liege region cross departments, in order to set up the QA processes, create hardware and software testing tools, set up templates...
Medical devices testing & validation - Wallonia
Are you looking to work into medical devices testing and validation? One of my client is interested to have someone on a contracting basis... to work in Liege region cross departments, in order to set up the QA processes, create hardware and software testing tools, set up templates...
Medical devices testing and validation Wallonia
Huxley Associates - België
Are you looking to work into medical devices testing and validation? One of my client is interested to have someone on a contracting basis... to work in Liege region cross departments, in order to set up the QA processes, create hardware and software testing tools, set up templates...
Medical devices testing & validation - Wallonia
One of my client is interested to have someone on a contracting basis to work in Liege region cross departments, in order to set up the QA...
QA / Validation Project Engineer / Project Manager (f/m)
NNE Pharmaplan - Brussel
complex field of pharma and biotech. We cover all segments from biopharmaceuticals and vaccines to medical devices and help our customers develop... sciences biotech industry biopharmaceuticals pharmaceuticals medical devices vaccins Belgium assurance qualit des normes gestion gnie ingnierie des...
Senior Manager Quality, JSC External Supply Integration
Johnson & Johnson Family of Companies - Beerse, Antwerpen
approach. * Master degree or higher . * In-depth knowledge and experience in Quality and/or Manufacturing in Pharma, Medical Devices & Diagnostics... with the QA counterparts at the External (Re-) Packers in the EMEA region. Adapt the quality overview approach as per the needs and maturity...
Biocartis - Mechelen, Antwerpen
Computer Science or equivalent by experience. At least five years’ experience in embedded software development including medical devices or in... design and development of medical devices or in-vitro diagnostic equipment working within an ISO13485 / GMP compliant environment Perfect English...
Biocartis - Mechelen, Antwerpen
compliant with the requirements of the Biocartis QMS with regards to FDA / CE requirements for In-Vitro Diagnostic (IVD) medical device regulations... in conjunction with the QA/RA team. Contributing to the materials review processes for disposition of rejected or scrapped parts through the...
compliant with the requirements of the Biocartis QMS with regards to FDA / CE requirements for In-Vitro Diagnostic (IVD) medical device regulations... in conjunction with the QA/RA team. Contributing to the materials review processes for disposition of rejected or scrapped parts through the...
ClearSource–7665– Software Quality Officer (m/f)–permanent
ClearSource - Brussel
; of hardware & software) - Experience in QA of safety critical systems is an asset (e.g. medical devices, aircraft..., and you oversee system testing activities ensuring certification according to the applicable regulations. You also assist the R&D QA manager in...
in a manufacturing organization producing medical devices, pharmaceuticals or in-vitro diagnostic equipment working within an ISO 13485 / GMP...’ experience working in a manufacturing organization producing medical devices, pharmaceuticals or in-vitro diagnostic equipment working within an ISO...