the world’s first real-time artificial intelligence medical device that is globally distributed by Medtronic.
About the role
Member of the Regulatory Affairs department cooperating in regulatory submissions and registrations, periodic reports...
Sei pronto per entrare a far parte di una società di consulenza leader mondiale nell'industria farmaceutica e dei Medical Device? PQE Group è affermata in questo settore dal 1998, garantendo una presenza internazionale grazie alle 45 filiali...
the world’s first real-time artificial intelligence medical device that is globally distributed by Medtronic.
About the role
Member of the Regulatory Affairs department cooperating in all aspects of the activities related to compliance with...
On behalf of our Client - Ipsen, a global biopharmaceutical company focused on innovation - IQVIA is looking for a Medical Science Liaison.
As part of the MedicalAffairs department, the MSL is a field-based scientific expert to external...
Po 9 Rome, Italy
Workplace: Office-based / availability to travel
The Regulatory Affairs Manager oversees the regulation process for products (Medical Device and Marketing Authorization) requiring governmental approval...
and help in developing medical material and resources.
• Support interventional and non-Interventional clinical trials in close collaboration with Clinical development, Clinical Operations and Global MedicalAffairs teams. Ensure a strategic approach to...
Opportunità
Il nostro cliente è una multinazionale del settore farmaceutico in fase di lancio di prodotti innovativi in ambito oncologico.
Per loro conto siamo alla ricerca di un MSL che entrerà a far parte del dipartimento MedicalAffairs...
the pharmaceutical, biotech, and medical device industries globally. PharmaLex is specialised in effectively designing all aspects of drugs and medical devices regulatory needs, ranging from early development and market entry to product maintenance...
Junior Regulatory Affairs Specialist of Cosmo Intelligent Medical Devices.
Work Location: Rome – Italy – Viale Ostiense 131/L
Key Responsibilities:
1. Assess, prepare, and manage technical documentation to support certification and submission...
Join the Quality Service Operations team to uphold the highest standards of quality and compliance in post-market support, ensuring exceptional service and reliability for life-saving medical devices.
Work Location: Rome – Italy – Viale Ostiense...
Join the Quality Production Operations team to drive excellence in manufacturing and ensure the highest standards of quality and compliance in the production of advanced medical devices.
Work Location: Rome – Italy – Viale Ostiense 131/L
Key...
and best practices within the Italian team and within the INT region.
• Proactively coordinate collaboration with medicalaffairs and market access (and other internal stakeholders) to ensure alignment in objectives and activities with accounts and external...
requirements.
3. External intelligence: Identifying the most recent regulatory trends, share insights and lessons learned across the European region, and collaborating in consultation process in close partnership with Government Affairs and GCO.
4. Managing...