Fda Regulations Jobs in Livorno

Apple is looking for a qualified and motivated silicon validation engineer. You will be part of a team doing pre/post-silicon bring- up debug validation and characterisation of analog and mixed signal Power Management circuits for battery operated portable position is for an engineer More...

Main Purpose of Role: Maintenance of the NB 1639 medical device internal quality management system. Managing of daily QA tasks:Updating and maintenance of documents under the MDD MDR and IVDR schemeManagement the IF databaseCollaboration on generic scheme documentsPublishing of docume More...

Please submit your CV in English.You will contribute to statistical programming activities related to global clinical trials work closely with international teams of statisticians programmers and data managers program data sets and summaries.You will:Develop analysis data se More...

Main Purpose of RoleTo centrally manage a Lean and compliant Quality Management system for medical devices schemes (Medical includes Notified Body NB1639 UKCA ISO 13485 MDSAP and all other Medical Schemes at SGS)Management of external audits and communication with competent authorityM More...

 We are seeking a highly skilled Regulatory Manager to oversee the clinical and performance evaluation components of our medical device conformity assessment process within Notified Body 1639. This role is vital to ensuring regulatory excellence clinical integrity and t More...