Drug Surveillance Specialist

Associate MDR/Vigilance SpecialistAbout the RoleThis entry-level position involves monitoring our drug or medical devices surveillance program including the intake, protocol development, evaluation, processing, and follow-up on adverse reports.The successful candidate will participate in the resolution of any legal liability and ensure compliance with...

Medical Devices Surveillance Program SpecialistWe are seeking a highly skilled Medical Devices Surveillance Program Specialist to join our team. As a key member of our surveillance program, you will be responsible for ensuring compliance with government regulations and developing protocols for adverse report intake, evaluation, and follow-up.About the...

Associate MDR/Vigilance SpecialistResponsibilities- Monitors the company's drug or medical devices surveillance program including the intake, protocol development, evaluation, processing, and follow-up on adverse reports.- Participates in the resolution of any legal liability and ensures compliance with government regulations.- Ensures complete and accurate...

Associate MDR/Vigilance SpecialistResponsibilitiesMonitors the company's drug or medical devices surveillance program including the intake, protocol development, evaluation, processing, and follow-up on adverse reports.Participates in the resolution of any legal liability and ensures compliance with government regulations.Ensures complete and accurate...

Job Title: Senior Design Quality Assurance EngineerAbout Your New Role:As a Senior Design Quality Assurance Engineer, you will lead design quality projects related to the drug-coated balloon product line, ensuring compliance with internal and regulatory requirements.Your Responsibilities Will Include:Leading design quality projects and ensuring compliance...

Social network you want to login/join with:Senior Supervisor Design Quality Assurance, GalwayLocation: Galway, IrelandJob Category: OtherEU work permit required: YesJob Reference: 19e0ded414aaJob Views: 8Posted: 10.08.2025Expiry Date: 24.09.2025Job Description:Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High PerformanceAt Boston...

Graduate Opportunity: Regulatory Affairs SpecialistFull time- Fixed Term (Maternity Contract)Galway- HybridAre you a recent graduate eager to kick-start your career in the medical device industry? Do you want to make a real impact in healthcare innovation while growing professionally in a supportive, dynamic environment?As a Graduate Regulatory Affairs...

Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High PerformanceAt Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges.With access to the latest tools, information and training,...

Press Tab to Move to Skip to Content LinkSelect how often (in days) to receive an alert: Create AlertSenior Design Quality Assurance EngineerOnsite Location(s):Galway, G, IEDiversity - Innovation - Caring - Global Collaboration - Winning Spirit - High PerformanceAt Boston Scientific, we'll give you the opportunity to harness all that's within you by working...

Join to apply for the Graduate Regulatory Affairs Specialist role at Veryan MedicalJoin to apply for the Graduate Regulatory Affairs Specialist role at Veryan MedicalGet AI-powered advice on this job and more exclusive features.Direct message the job poster from Veryan MedicalHR Coordinator, Veryan Medical | Assoc CIPD | MSc HRMGraduate Opportunity:...