Quality & Regulatory Lead – Medical Devices

A global manufacturing company in Italy is seeking a Quality and Regulatory Manager to oversee quality systems and regulatory compliance within the organization.The ideal candidate will have strong experience in quality engineering and regulatory affairs, particularly with ISO standards and FDA approvals.The role emphasizes continuous improvement through...

A leading medical device firm in Italy is seeking a Regulatory Affairs professional to support CE marking activities for medical devices.The role involves ensuring regulatory compliance, developing strategies, and collaborating with cross-functional teams.Ideal candidates will have 3-5 years of experience in Regulatory Affairs and possess a good...

Biopharmed è la boutique di head hunting progettata per la ricerca e selezione di profili tecnici e specialistici del mondo Life Sciences & Chemical.PosizioneRicerchiamo una figura da inserire nel team Regulatory Affairs for Medical Devices per importante azienda operante nel settore farmaceutico e del medical device.Principali ResponsabilitàCoordinamento...

A leading medical technology company is seeking an Advanced Regulatory Affairs Specialist in Rome, Italy.You will be responsible for regulatory activities related to product registrations and compliance across EMEA.The ideal candidate has a Bachelor's degree in Science or Engineering, at least 5 years of experience in regulatory affairs, and excellent...

A life sciences recruitment firm is seeking a Regulatory Affairs professional with at least 4 years of experience in the medical device sector.The role involves conducting regulatory assessments, managing registrations, and supporting FDA submissions.Excellent communication and problem-solving skills are essential, along with fluency in English.If you are...

The Director of Regulatory Affairs leads the global regulatory strategy of the MedTech AI Division, ensuring that all software and hardware products (SaMD, AI-enabled real-time systems, edge–cloud devices, imaging platforms, connectivity and data solutions) comply with U.S., EU, and international regulations.Reporting to the VP of Clinical Quality and...

A leading pharmaceutical company in Sicily is seeking a candidate to perform scientific information activities for physicians.This role requires a strong knowledge of regulatory requirements, excellent communication skills, and experience in the pharmaceutical or medical devices field.The ideal candidate will help enhance scientific efficacy in meetings and...

Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere.For 70 years our team has driven meaningful innovations in kidney care.As we build on our legacy we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services while...

Un'azienda nel settore Healthcare cerca un professionista per gestire audit e garantire la conformità alle normative ISO ***** 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...

A global pharmaceutical company is seeking a Medical Writer to support documentation throughout drug development.The successful candidate will prepare clinical study documents, perform quality control, and collaborate with cross-functional teams.Ideal applicants should have over 5 years of experience in medical writing, a relevant degree, and strong...