TRABAJO REGULATORY AFFAIRS MEDICAL DEVICE MADRID, MADRID

While part of the regulatory affairs organization, this role is not technical or strategic, but rather centered on routine administrative support to help ensure...

· regulatory compliance (change control, post-approval activities, etc... ?️ ticket restaurant? on-site medical service? benefits and savings club...

Experience with health care, business national/ regional legislative and executive branch regulatory and administrative processes/rules/systems...

Conduct regulatory intelligence gathering to support development of regulatory roadmaps, complex feasibility assessments, and other regulatory intelligence reports...

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...

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...

The ideal candidate will bring international experience, preferably from a medical device or healthcare company, or a law firm’s healthcare team...

Collaborates with local medical affairs team... works together with regulatory affairs to ensure timely delivery of application/documents for submissions to regulatory...

Services overview: local trial management services provides local management of a clinical trial (or medical affairs data generation activity) in a country or countries...

Understands regulatory guidelines and landscape... key responsibilities key member of the cross functional team & works closely with the cross functional brand team...

Follow quality and regulatory guidelines for medical device software development... complementary skillswould be a plus if you:exposure to software as medical device...

The project manager is responsible for maintaining the proper project documentation and ensuring compliance with sops and regulatory requirements for clinical...

Follow quality and regulatory guidelines for medical device software development... nice to have:â exposure to software as medical deviceâ ... intermediate to upper-intermediate...

Advise on regulatory interactions, support successful management of regulatory examinations and requests; conduct regulatory horizon scanning...

Company description sobi offers the opportunity to work at an international pharmaceutical company focused on specialty pharmaceuticals meeting the high medical...

•    in-depth knowledge of european pricing mechanisms and regulatory frameworks (e...     •    establish and maintain strong relationships with external stakeholders...