Regulatory Project Manager—Medical Devices Compliance

A leading medical device manufacturer is seeking a Temporary Project Manager to ensure regulatory compliance for EU medical devices. This role requires strong leadership, project management experience, and fluency in Italian. The successful candidate will coordinate multidisciplinary teams and manage the compliance action plan while adhering to tight...

Overview Alchimia is one of the leading European manufacturers of medical devices for ophthalmic surgery and tissue banks. With our expertise in chemistry, microbiology, and pharmacology, at Alchimia we have adopted this rule: we design each medical device as if it were intended for ourselves. Since our foundation in 1993, all our products have been...

Overview Alchimia is one of the leading European manufacturers of medical devices for ophthalmic surgery and tissue banks. With our expertise in chemistry, microbiology, and pharmacology, at Alchimia we have adopted this rule: we design each medical device as if it were intended for ourselves. Since our foundation in 1993, all our products have been...

Overview Alchimia is one of the leading European manufacturers of medical devices for ophthalmic surgery and tissue banks. With our expertise in chemistry, microbiology, and pharmacology, at Alchimia we have adopted this rule: we design each medical device as if it were intended for ourselves. Since our foundation in 1993, all our products have been...

OverviewAlchimia is one of the leading European manufacturers of medical devices for ophthalmic surgery and tissue banks. With our expertise in chemistry, microbiology, and pharmacology, at Alchimia we have adopted this rule: we design each medical device as if it were intended for ourselves.Since our foundation in 1993, all our products have been developed...

OverviewAlchimia is one of the leading European manufacturers of medical devices for ophthalmic surgery and tissue banks. With our expertise in chemistry, microbiology, and pharmacology, at Alchimia we have adopted this rule: we design each medical device as if it were intended for ourselves.Since our foundation in 1993, all our products have been developed...

Un'azienda nel settore Healthcare cerca un professionista per gestire audit e garantire la conformità alle normative ISO 13485 e MDR. Richiesta laurea in discipline scientifiche e almeno 5 anni di esperienza in Quality Assurance nel settore medical device. È fondamentale la conoscenza dell'inglese e capacità di lavorare in autonomia. Offrono contratto a...

Global Regulatory Intelligence & Compliance SpecialistAre you looking for a new challenge? Do you like dealing with regulations, standards, and global compliance? If yes, take a look: this could be for you!Clivet SpA is now looking for a dynamic and proactive Global Regulatory Intelligence & Compliance Specialist to join our dynamic team.This role will be a...

Global Regulatory Intelligence & Compliance SpecialistAre you looking for a new challenge? Do you like dealing with regulations, standards, and global compliance? If yes, take a look: this could be for you!Clivet SpA is now looking for a dynamic and proactive Global Regulatory Intelligence & Compliance Specialist to join our dynamic team.This role will be a...

Global Regulatory Intelligence & Compliance SpecialistAre you looking for a new challenge?Do you like dealing with regulations, standards, and global compliance?If yes, take a look: this could be for you!Clivet SpA is now looking for a dynamic and proactiveGlobal Regulatory Intelligence & Compliance Specialistto join our dynamic team.This role will be a key...