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Summary The RA specialist drives and/or supports key MMS projects in which regulatory affairs is a critical component or driver. This role applies to a broad portfolio of products including Infusion Pumps (Programmable Electrical Medical Devices), stand-alone software as medical device, and dispos...
Regulatory Affairs Manager - Manchester - 65k+ An exciting opportunity has arisen with a well established Diagnostics group for a Regulatory Affairs Manager to join the team. This role will support effective management of the companies Regulatory Affairs strategy, which will impact the global commer...
Job TitleNorm Compliance OfficerJob DescriptionIn this role, you have the opportunity to design, develop and maintain Diagnostic X-ray systems (Radiography, Fluoro Mammography) and realization of a range of products in such a way that future products options and features can be realized with accepta...
Im currently working with a leading medical device company located in Limerick who are looking for an RA specialist to join their team. The RA specialist supports a broad range of projects for the companies devices. You will participates in cross-functional teams as the regulatory expert (e.g. new p...
Role: Senior Design Assurance EngineerIndustry: Medical DevicesLocation: GalwayA key client of ours have just released a new role on their team for an experienced Design Assurance Engineer. The ideal candidate will have 5+ years experience in a medical device manufacturing environment with direct ex...
02. Quality Assurance and Regulatory Manager - Position OPEN Desired qualifications Bachelor s Degree in Engineering, Science, or health-related field Minimum Requirements Working knowledge of CE,FDA and other regulatory authorities FDA Regulatory submission experience (510ks, PMAs, IDEs) Quality ...
I am currently looking for a Quality Engineer for a company based in Sligo. The successful Quality Engineer would be working for world leader in the manufacture of medical devices. You must have had experience of working within the QMS and contribute to the maintenance of the QMS. Responsibilities:C...
Desired qualificationsBachelors Degree in Engineering, Science, or health-related fieldMinimum RequirementsWorking knowledge of CE,FDA and other regulatory authoritiesFDA Regulatory submission experience (510ks, PMAs, IDEs)Quality Systems development, implementation, and training experienceExperienc...
Lead, plan, develop and direct establishment and continual improvement of the Quality Systems and quality assurance standards to ensure compliance with US and international regulations and standards. Direct activities of the Quality Assurance, organization and personnel. Serve as the company's Manag...
PEGA DEVELOPERKnowledge Expert is looking for highly motivated, innovative and forward thinking talent to join our family and continue making a major impact on how large organizations transform and deliver tangible business results with Software.Being a consultancy, our teams work on a huge variety ...
