TRABAJO REGULATORY AFFAIRS MEDICAL DEVICE BARCELONA, BARCELONA
(29 ofertas de trabajo)
Listado de trabajos de Regulatory affairs medical device en Barcelona, Barcelona
Regulatory affairs medical devices
Experiencia previa en posición similar con medical devices de entre 1 y 3 años... si crees que tu perfil puede encajar y tienes ganas de iniciar un nuevo proyecto...
Medical safety lead / sr medical safety lead (crm)
medical records... regulatory compliance... medical strategy... medical information... collaborates productively on clinical safety tasks with colleagues from clinical...
Global medical director, metabolics plus
Position: global medical director, metabolics plus location: barcelona - spain (3 days working from the office and 2 days working from home) this is what you will...
Country regulatory affairs)... medical affairs, commercial, clinical development, cmc)... the senior regulatory affairs specialist, international regulatory affairs...
R+d project leader (medical devices)
Lead the device verification stage and generate the necessary documentation to present to the regulatory body... main responsibilities:lead the development of a...
Support the regulatory submissions for market authorization for medical device products... oversee post-market surveillance activities related to medical device...
Senior specialist, pharmacovigilance
We cover all therapy areas including medical device... job description the senior specialist, regulatory and pv network is responsible for developing the strategy...
Data and algorithm development engineer
Innitius is an innovative medical device company focused on women’s health... prepare regulatory documentation and design processes with the quality and regulatory...
Our state-of-the-art, dog-friendly campus includes a medical center, canteen, and collaborative spaces for networking and relaxation... we encourage the diversity...
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Validation of pharmaceutical computerized systems
With offices in barcelona, the uk, and china, we support the pharmaceutical, biotech, and medical device supply chains globally... engaging in international projects:contribute...
Develop all activities in compliance with gcp and under an ethical and regulatory frame... prepare study documentation for fda pre-submissions and submissions, and...
Experience in all study phases and in rare medical conditions preferred... good medical knowledge and ability to learn relevant alexion therapeutic areas...
Support regulatory submissions, respond to queries, and present at regulatory meetings... clinical research and clinical development experience required (cra) (>10...
Responsibilities key accountabilities • acts as key marketing technical liaison on all given product lines, providing product and regulatory information to sales...
Associate director, senior patient safety scientist oncology
regulatory reports, health authority responses and the safety content of marketing authorisation applications... patient safety sits within the chief medical office...
Additional skills/knowledge: knowledge about applicable standards and regulations related with sw development for health and/or medical device...
Accountabilities: • demonstrate independence in providing statistical support for standard design and interpretation of study data • under guidance of a more experienced...
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