TRABAJO REGULATORY AFFAIRS MEDICAL DEVICE MADRID, MADRID
(21 ofertas de trabajo)
Listado de trabajos de Regulatory affairs medical device en Madrid, Madrid
· regulatory compliance (change control, post-approval activities, etc... ?️ ticket restaurant? on-site medical service? benefits and savings club...
Director government affairs spain and portugal
Experience with health care, business national/ regional legislative and executive branch regulatory and administrative processes/rules/systems...
Principal regulatory strategist (cro/pharma industry) - europe
Conduct regulatory intelligence gathering to support development of regulatory roadmaps, complex feasibility assessments, and other regulatory intelligence reports...
Medical scientific liaison (msl) oncology
At least 1 year of medical affairs or msl experience... the medical scientific liaison (msl) role is a position specifically designed to meet the needs of scientific...
Clinical research associate (cra) - madrid (hybrid)
Why join us? this is a great opportunity to build deep expertise in site start-up and regulatory affairs at a leading medical device company...
Product assessor / senior product assessor - sterilization
Work proactively to minimize risks associated with medical device certifications... responsibilities: conduct comprehensive sterilization product assessments in...
The ideal candidate will bring international experience, preferably from a medical device or healthcare company, or a law firmâs healthcare team...
Local study associate director
Collaborates with local medical affairs team... works together with regulatory affairs to ensure timely delivery of application/documents for submissions to regulatory...
In our european consumer compliance organization, we are looking for a compliance analyst to join our european payments regulatory compliance team...
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Local clinical trial manager - fsp - inmunology
Services overview: local trial management services provides local management of a clinical trial (or medical affairs data generation activity) in a country or countries...
Follow quality and regulatory guidelines for medical device software development... complementary skillswould be a plus if you:exposure to software as medical device...
Understands regulatory guidelines and landscape... key responsibilities key member of the cross functional team & works closely with the cross functional brand team...
Contributing strategic insights across clinical development, regulatory, market access, and medical affairs functions... applying advanced statistical methodologies...
Advise on regulatory interactions, support successful management of regulatory examinations and requests; conduct regulatory horizon scanning...
Clinical project associate in spain
A minimum of 4 years’ experience in clinical operations in biopharmaceutical/medical device industry, including site management and monitoring...
Expert c++ developer (3d, aws)
Follow quality and regulatory guidelines for medical device software development... nice to have:â exposure to software as medical deviceâ ... collaborate with multi-disciplinary...
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