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RegulatoryAffairs Manager - Medical Devices, Food Supplements & Cosmetics
La figura, inserita nel team Regulatory , avrà un ruolo chiave nel garantire la conformità normativa internazionale , supportare lo sviluppo e la registrazione dei prodotti nei vari...
ALTEN Italia è alla ricerca di un professionista con almeno 10 anni di esperienza in RegulatoryAffairs, con una solida esperienza nella gestione della conformità normativa per dispositivi medici e dispositivi di somministrazione dei farmaci.
Sede...
Adecco Italia ricerca per azienda cliente specializzata nella commercializzazione di oli e grassi lubrificanti , un /a perito chimico.INDUSTRIA CHIMICA/ CHIMICA-FARMACEUTICA Citt : Milano (Milano) Esperienza lavorativa: Regulatoryaffairs specialist...
ALTEN Italia è alla ricerca di un professionista con almeno 10 anni di esperienza in RegulatoryAffairs, con una solida esperienza nella gestione della conformità normativa per dispositivi medici e dispositivi di somministrazione dei farmaci.
Sede...
a RegulatoryAffairs Specialist with strong expertise in MDR and technical documentation preparation.
Main Responsibilities
• Prepare and maintain the Technical Documentation (TD) and Design Dossiers in compliance with EU MDR 2017/745, especially for Class...
development.Collaborate with Business Development to grow and optimize the product pipeline.Organize and lead cross-functional LEAP teams for project execution.Act as the strategic interface between internal departments including RegulatoryAffairs, Medical, R&D...
a RegulatoryAffairs Specialist with strong expertise in MDR and technical documentation preparation.
Main Responsibilities
Prepare and maintain the Technical Documentation (TD) and Design Dossiers in compliance with EU MDR 2017/745 , especially for Class...
departments including RegulatoryAffairs, Medical, R&D, and Sales.
• Build and maintain strong relationships with Key Opinion Leaders (KOLs) and external agencies.
Requirements:
• At least 3 years of experience in product management.
• Degree in Pharmacy...
a RegulatoryAffairs Specialist with strong expertise in MDR and technical documentation preparation.
Main Responsibilities
• Prepare and maintain the Technical Documentation (TD) and Design Dossiers in compliance with EU MDR 2017/745, especially for Class...
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 professional who dares to look outside the...
affairs in BD and ROW development including new and lifecycle management programs.
Build and maintain close collaboration with internal stakeholders (Preclinical Research, Toxicology, DMPK, Regulatory, ClinOps, Project Management, Medical Affairs, legal...
2 offerte simili: Sant'Ambrogio di Torino, Casalnuovo di Napoli
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 professional who dares to look outside the...