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238 Fda Jobs

Quality Technician - North Dublin Leinster, Ireland Management system processes within an ISO 13485 & FDA 21 CFR Part 820 regulatory environment. Core Responsibilities: • Responsible for technical inspection of electro-mechanical parts & instrumentation Yesterday
Senior R&D Manager/Director Dublin, County Dublin, Ireland in compliance with applicable FDA and ISO standards and regulations CFR as well as MDD provides the foundation for this role. Role/Responsibilities: Manage our multi-disciplinary and multi-site R&D hardware team 6 days ago
Verification and Validation Test Engineer Reperio Human Capital - Dublin Verification and Validation Test Engineer - Dublin, €80,000-€90,000 I have partnered with Medical Device Start-Up coming with FDA backing for two current top of the range products to assist £69059 - £77691/annum healthcare, hybrid 10 days ago
Senior Project Engineer Cork, County Cork, Ireland device directive (ISO13485, MDD and FDA CFR 820) and other pertinent Design Control requirements. #J-18808-Ljbffr 4 days ago
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Senior Regulatory Affairs Specialist - SH Medtronic Vascular Galway UC - Galway, County Galway, Ireland decisions. Ability to comprehend principles of engineering, physiology, and medical device use. You collaborate with global cross functional teams and create alignment with team members. Experience with FDA 3 days ago
Mes recipe author Opus Recruitment Solutions - London : Diploma qualification in suitable science/engineering course and/or suitable experience. Job/Technical Skills A minimum of 5 years’ experience in Batch processing operations in an FDA/ HPRA regulated £80 - £90/hour Remote 7 days ago
Director of Quality Galway, County Galway, Ireland engagement across multiple sites in the business to support common customer programs and medical device platform alignment. Provides quality system compliance with major Regulatory Authorities (U.S. FDA 9 days ago
Lead CQV Consultant Leinster, Ireland , Qualification and Validation of the project •Documentation preparation of Commissioning, Qualification & Validation documentation •Review of Contractor Handover Packages. •Knowledge of regulations (ICH, ASTM, FDA 5 days ago
Validation Engineer Headcount Solutions Limited - Sligo, Sligo County and active participation in the validation of site equipment, facilities, utilities, processes and software in compliance with company policies, FDA, * European cGMP and GAMP standards. * Generation 13 days ago
Senior Operations Manager Ireland .) compliance with Food and Drug Administration (FDA), British Standards Institution (BSI), Equal Employment Opportunity (EEO) regulations etc Develops, communicates and builds consensus for operating goals Yesterday

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