Regulatory Compliance specialist or Manager (MDR & ISO 13485)
... 2 years of experience in regulatory affairs within the medical device industry. Detailed knowledge of MDR ...
... 2 years of experience in regulatory affairs within the medical device industry. Detailed knowledge of MDR ...
... of 6+ years of related Regulatory Affairs experience within Medical Device is required (4+ years with Advanced Degree).brExperience with medical device regulatory new product submissions required.brA ...
... stages as well as regulatory submissions.Specific responsabilitiesSearch and selection of new technologies, suppliers and CDMOs for the development and assembly of medical devices.Collaborate in generation of medical devices Design History File (DHF ...
... stages as well as regulatory submissions.Specific responsabilitiesSearch and selection of new technologies, suppliers and CDMOs for the development and assembly of medical devices.Collaborate in generation of medical devices Design History File (DHF ...
... of 4+ years of related Regulatory Affairs experience within Medical Device is required (3+ years with Advanced Degree).brExperience with medical device regulatory new product submissions required.brA ...
... conducted by external providers or regulatory agencies. Key Activities: Lead the ... preference for experience within the medical device industry . In-depth knowledge of ...
... role of Director, Immunology European Medical Engagement Lead (MEL) is to ... Leaders should be aligned with medical strategies, and the role should ... Practices and ethical, governmental, and regulatory requirements. Understands treatment paradigms and ...
... be the appropriate medical service for the childPrepares medical reports. Consults with Case Coordinators, ... assurance team: Participates with Medical Record Review,Video Conferencing and ... and directives from the Medical Director and Division Chief. Under ...
... submitted in time to ensure regulatory compliance.Specific Responsibilities:Prepare the ... procedures.Make sure that the regulatory database is up to date ... up to date on latest regulatory requirements related to post-marketing ...
... statute. Determinessituations requiring a medical examination or further testing hospital ... positive andnegative findings. Prepares medical reports. Consults with Case Coordinators, ... in need of further medical care and services. Provides depositions ...