Medical Device Development Specialist

Job Title: Senior Medical Device Development SpecialistThis role is for a highly skilled specialist to join our team on a permanent basis.The position involves leading the design, development and performance evaluation of drug-device combination products ensuring they meet regulatory standards.Provide technical expertise to support the development of...

Senior Medical Device Development SpecialistWe are seeking a highly skilled professional to lead the design, development, and performance evaluation of drug-device combination products in our team in Dublin.About the Role:The successful candidate will provide subject matter expertise to support formulation and manufacturing development activities for...

Medical Device Manufacturing SpecialistA Medical Device Manufacturing Specialist is responsible for developing, implementing, and optimizing high-performance manufacturing processes for medical devices.Main Responsibilities:Design and develop advanced manufacturing processes for medical devicesCollaborate with cross-functional teams to support new product...

Lead Medical Device Development SpecialistWe are seeking an experienced medical device development expert to oversee the design, testing and evaluation of drug-device combination products.Develop subject matter expertise for Combination Product developmentPlan and execute design verification and reliability strategiesDesign test methods and specifications to...

Program Management RoleAs a seasoned Program Manager, you will be responsible for overseeing the success of strategic projects and initiatives within the medical device industry. You will lead cross-functional teams, ensuring alignment with business goals, and deliver innovative medical devices that enhance patient care.Lead Multiple Programs: Manage...

Job SummaryThe role of Regulatory Affairs Specialist is crucial for the post-market activities of medical devices, supporting departmental regulatory processes and procedures, strategies, authoring, reviewing, and supporting global registrations.Main Responsibilities:Support regulatory strategies for OUS medical devices and combination products, ensuring...

Job OverviewWe are seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our organization, you will be responsible for post-market activities for medical devices.This role requires a strong understanding of global device adverse event/incident reporting requirements, with a focus on US, EU and international...

Job Title: Clinical Regulatory SpecialistThe role of a Clinical Regulatory Specialist is pivotal in the development of innovative medical devices. Key responsibilities include supporting design development, verification, clinical trials, validation, and regulatory approval.Key ResponsibilitiesCoordinate global clinical trial execution, including site...

Regulatory Specialist for Medical DevicesThis position requires a subject matter expert in the application of FDA, EU and ISO standards, regulations and guidance related to design control and regulatory compliance.The successful candidate will maintain detailed awareness and understanding of current regulations and regulatory guidance in regions of interest...

This role is ideal for individuals with a strong foundation in engineering or science, seeking to contribute to the development of cutting-edge medical devices.Key ResponsibilitiesAs a key member of our R&D team, you will be responsible for sourcing and building prototypes, testing methods, and analyzing data to identify optimal solutions.You will develop...