La/Il RegulatoryAffairs Specialist lavorerà nella funzione del Regolatorio di Alifax Srl. Siamo alla ricerca di una risorsa con almeno due (2) anni di esperienza maturata presso aziende del settore dispositivi diagnostici in vitro.
La risorsa...
Overview
Sr Specialist, Global Regulatory AffairsHerbalife Italy – RomeVia Amsterdam, 125Roma00144
About the role:We’re looking for an experienced Senior Specialist, Global RegulatoryAffairs to join our dynamic Global RegulatoryAffairs team...
Medical Manager (Northern Italy)
About the role
For our dynamic growing, innovative Brands division within an already established big generic International pharmaceutical company, we are looking for an experienced Medical Affairs field...
Junior RegulatoryAffairs 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...
customers and drive improvements within the retail industry. We're looking for a high-judgement and self-motivated individual' with experience bridging business needs' high-value communications' and government or regulatory environments' to work on global...
Senior RegulatoryAffairs Specialist of Cosmo Intelligent Medical Devices.
Work Location: Rome – Italy – Viale Ostiense 131/L
Key Responsibilities:
• Assess medical device safety by providing input/review to the risk management activities...
Overview
Grow with us. Do you thrive in complex, fast-paced environments? Are you a legal leader who can navigate ambiguity with creativity and a global perspective? If so, this role may be your next step! Our Group Function Legal Affairs...
and Clinical Affairs
• Report directly to the President, providing regular updates on performance and market trends
Requirements
• Minimum 10 years of experience in sales, with at least 5 in a leadership role
• Proven ability to manage and develop high...
Rud Pedersen Public Affairs office in Brussels opened in 2017 and has grown consistently with around 75 team members today. In response to evolving client needs, we are looking for a Research Executive to strengthen our team and support our growing...
correctly carried out and registered.
6. Training: Ensure that the training and guidance to external parties are correctly registered.
7. Compliance: Support the RegulatoryAffairs in compliance with all relevant regulations, including FDA, ISO, and other...
production staff are correctly registered
• Design transfer: ensure that the design transfer activities are correctly carried out and registered
• Compliance: Support the RegulatoryAffairs in the compliance with all relevant regulations, including FDA, ISO...
products and ensure that all regulatory requirements are met and aligned with local and Global standards.
• Maximize your skills in critically analyzing and interpreting clinical trial data, real-world evidence, and scientific literature. You will...
integrity across cleanrooms and manufacturing areas* Coordinate validation activities and maintain change control documentation* Interface with regulatoryaffairs teams and support inspection readiness* Implement risk-based compliance monitoring...