Regulatory Affairs 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
Regulatory Affairs 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...
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...
Alchimia srl-Ponte San Nicolò, 7 km da Maserà di Padova
Regulatory Affairs 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...
International Clinical Specialist
Are you ready to make a meaningful impact in the world of medical innovation while advancing your career in a dynamic, global role?
Our client, a leader in medical device innovation, is seeking an International...
Alchimia srl-Ponte San Nicolò, 7 km da Maserà di Padova
a Regulatory Affairs 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...
Regulatory Affairs 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...
a Regulatory Affairs 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...
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