RegulatoryAffairs Specialist
Alchimia is one of the leading European manufacturers of medical devices for ophthalmic surgery and tissue banks. With strong expertise in chemistry, microbiology, and pharmacology, we develop every product with...
Alchimia srl-Ponte San Nicolò, 7 km da Maserà di Padova
RegulatoryAffairs Specialist
Alchimia is one of the leading European manufacturers of medical devices for ophthalmic surgery and tissue banks. With strong expertise in chemistry, microbiology, and pharmacology, we develop every product with...
le tue capacità di adattabilità e project management per adattarti rapidamente ai cambiamenti della consulenza, consentendoti di affrontare sfide sempre diverse
Opportunità di viaggiare a livello nazionale e internazionale
Il nostro Team di RegulatoryAffairs...
Alchimia srl-Ponte San Nicolò, 7 km da Maserà di Padova
RegulatoryAffairs Specialist
Alchimia is one of the leading European manufacturers of medical devices for ophthalmic surgery and tissue banks. With strong expertise in chemistry, microbiology, and pharmacology, we develop every product with...
RegulatoryAffairs Specialist
Alchimia is one of the leading European manufacturers of medical devices for ophthalmic surgery and tissue banks. With strong expertise in chemistry, microbiology, and pharmacology, we develop every product with...
ADECCO ITALIA S.p.A.-Padova, 10 km da Maserà di Padova
La divisione specializzata Adecco LifeScience ricerca, per conto di un'importante azienda operante nel settore Medicale, un/una:
REGULATORYAFFAIRS Specialist
La realtà in questione è un'azienda italiana con sede in provincia di Padova, leader...
Alchimia srl-Ponte San Nicolò, 7 km da Maserà di Padova
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...
La divisione specializzata Adecco LifeScience ricerca, per conto di un'importante azienda operante nel settore Medicale, un/una:
REGULATORYAFFAIRS Specialist
La realtà in questione è un'azienda italiana con sede in provincia di Padova, leader...
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...
Hitachi Vantara Corporation-Monselice, 13 km da Maserà di Padova
Your background
• Bachelor’s or Master’s degree in Environmental Science, Sustainability, Engineering, or a related field.
• Proven experience of environmental impact assessment, sustainability, or regulatoryaffairs within the transformers, electrical...
providers.
Support regulatoryaffairs by ensuring all clinical and engineering documentation is complete and accurate for regulatory submissions.
Provide on-site and remote support during pre-clinical and clinical procedures.
What We’re Looking For...
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...
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...