Medical Device Specialist

Job Opportunity in Product DevelopmentWe are seeking an experienced engineer to join our team as a product development specialist. This role will involve developing and delivering complex projects, working collaboratively with cross-functional teams, and ensuring robust product design.The successful candidate will have a strong background in mechanical or...

Medical Device Sourcing SpecialistJob Overview:The Medical Device Sourcing Specialist is responsible for managing all aspects of sourcing and materials planning related to new product development & production of early stage medical devices.This position will collaborate with cross-functional teams, including Design Engineering, Program Management, Quality,...

Key Position: Mechanical EngineerWe are seeking a highly experienced Lead Mechanical Engineer to join our specialist R&D division. The ideal candidate will have a proven track record in medical device development and be proficient in SolidWorks or CREO.Job Responsibilities:Design and develop complex mechanical systems for medical devices.Lead...

Lead Quality Assurance SpecialistAbout the RoleThe Lead Quality Assurance Specialist will be responsible for ensuring the highest quality of medical devices, adhering to regulatory requirements and industry standards. This role involves collaborating with cross-functional teams to develop sterile and non-sterile medical devices.Main ResponsibilitiesRisk...

Job DescriptionA highly experienced Regulatory Affairs Specialist is sought to join a key role in Galway.This role will work closely with cross-functional teams to obtain regulatory approvals for a new medical device therapy.Support and advise the Quality leadership on regulatory activities and strategies.Develop and submit high-quality regulatory documents...

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...

Compliance Specialist for Medical Device ManufacturingWe are seeking a Compliance Specialist to support our remediation program following an FDA 483 observation. The ideal candidate will have experience in medical device manufacturing and quality management, with a strong understanding of process validation and CAPA/NCR management.Main...

We are seeking a Manufacturing Specialist to join our team. As a manufacturing specialist, you will work in a cleanroom environment where you will be responsible for assembling and inspecting parts in the manufacture of medical devices products.Your responsibilities will include:

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...

Regulatory Affairs SpecialistJob Description:The Regulatory Affairs Specialist will be responsible for managing the regulatory and vigilance process, preparing regulatory submissions, maintaining technical files, and supporting quality and regulatory management.Manage the regulatory and vigilance process to ensure compliance with EU, UK, and FDA...