Regulatory Strategy Lead, AI/ML Medical Devices
il y a 5 heures
A cutting-edge medical technology firm in Paris seeks an experienced Regulatory Affairs professional to develop innovative regulatory strategies for AI/ML-enabled medical devices. This role involves preparing submissions, serving as a liaison with regulatory bodies, and ensuring compliance. Ideal candidates will have over 6 years of relevant experience, strong communication skills in English and Korean, and a Bachelor's degree in a relevant discipline. A competitive salary package is offered, alongside opportunities for international relocation.
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Chargé D'affaires Réglementaires
il y a 6 jours
Paris, France BIORIUS - Your cosmetic regulatory expert Temps plein**About BIORIUS** **About the Position** Historically focused on human health, BIORIUS is adapting to the new constraints and opportunities suggested by its market. The Medical Device business unit recruits a Regulatory Affairs / Quality Specialist. Since many developments are expected and capacity building is needed, this position requires a senior...
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Regulatory Affairs Specialist
il y a 1 semaine
Paris 4e, France VIQI Temps plein**Your responsibilities** - Maintaining the Technical Documentation for Medical Devices with support of other functions - Becoming familiar with regulations and standards applicable to specific areas of responsibility, which may include notified body exposure - Support product registrations including document management - Support the Medical Device team in...
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Lead - Regulatory Information Management
il y a 1 semaine
Paris, Île-de-France Weekday AI Temps pleinThis role is for one of the Weekday's clientsMin Experience: 8 yearsLocation: EuropeJobType: full-timeWe are seeking an experienced Veeva Regulatory Information Management (RIM) professional with strong expertise in Ennov to lead and support global regulatory operations and system implementations. The ideal candidate will play a critical role in managing...
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Regulatory Affairs Manager
il y a 8 heures
Paris, France elemed Temps pleinOverviewTitle: Senior Consultant – Device Regulatory Documentation & ComplianceLocation: Paris (3 days onsite - 2 WFH)The CompanyWe believe great work happens when brilliant minds come together with a shared purpose. This biopharma company is known for its dedication to employee happiness, its collaborative environment, and its passion for bringing...
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Head of Clinical Operations — Global MedTech Trials Lead
il y a 11 heures
Paris, France HEPTA Medical Temps pleinA fast-growing MedTech company in Paris is seeking a Head of Clinical Operations to lead their clinical strategy and operations. The ideal candidate will have around 10 years of experience managing clinical trials within medical device companies and a strong regulatory background. Responsibilities include preparing clinical studies, managing submissions, and...
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Senior Regulatory Affairs Program Manager
il y a 23 heures
Paris, Île-de-France Sonio Temps pleinAbout SonioEach year, 140M children are born. Birth defects affect 1 in 33 births in developed countries, and in 50% of cases, they are not detected during prenatal examinations. Prenatal medicine is particularly complex, and the scans impose heavy responsibilities on healthcare professionals. They can also be a source of stress for future parents.Resulting...
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Senior Regulatory Affairs Program Manager
il y a 18 heures
Paris, Île-de-France Sonio Temps pleinAbout SonioEach year, 140M children are born. Birth defects affect 1 in 33 births in developed countries, and in 50% of cases, they are not detected during prenatal examinations. Prenatal medicine is particularly complex, and the scans impose heavy responsibilities on healthcare professionals. They can also be a source of stress for future parents.Resulting...
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Senior Project Manager
il y a 1 semaine
Paris 4e, France VIQI Temps pleinWe are actively looking to recruit a Senior Project Manager. This person will contribute to the development of new medical device solutions to address unmet clinical needs as part of the product development team. The Senior Project Manager will report to the Head of Product Development. RESPONSIBILITIES - Prepare, execute and monitor project plans to meet...
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Senior Regulatory Affairs Program Manager
il y a 8 heures
Paris, France Sonio Temps pleinAbout Sonio Each year, 140M children are born. Birth defects affect 1 in 33 births in developed countries, and in 50% of cases, they are not detected during prenatal examinations. Prenatal medicine is particularly complex, and the scans impose heavy responsibilities on healthcare professionals. They can also be a source of stress for future parents....
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Biologics CMC Regulatory Strategy Lead
il y a 9 heures
Paris, France Ipsen Group Temps pleinA leading biopharmaceutical company seeks a Senior Manager CMC Regulatory to oversee regulatory strategy for biological projects. This position involves coordinating with cross-functional teams, preparing submission dossiers, and ensuring compliance with international regulations. Candidates must have extensive experience in CMC regulatory affairs, a...