8 Medical Device Jobs in Clare
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Inspector - Evenings Shift Edwards Lifescience Ireland Ltd - Clare on Thursdays shift) Key Responsibilities: Perform visual, dimensional, and functional inspection on a wider variety of components and/or finished medical device products using a wide variety of tools 12000.0 Yesterday
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Senior Quality Specialist Cregg Group - Clare in medical device design, manufacturing, and distribution Key Responsibilities may include (but aren't limited to); Support the development, implementation, and maintenance of the Quality Management System 60000.0 10 days ago
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Quality Specialist Life Science Recruitment Ltd - Clare Medical Device company working on projects from concept. Summary: The Quality specialist role will involve supporting the development and implementation of the Quality Management System with my Medical 55000.0 13 days ago
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Quality Engineer Harmonics - Clare degree in a scientific discipline is an advantage Minimum of 3 years in a Quality Assurance role in Medical Device or Pharma is preferred. Excellent verbal and written communication skills Ability to work 45000.0 11 days ago
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Assoc. Assembler - Evening Shift Edwards Lifescience Ireland Ltd - Clare to complete assembly of medical devices precisely and in a timely fashion at each work station - proficient in multiple operations - following work order instructions and drawings, using computers to navigate 12000.0 19 days ago
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Senior Regulatory Affairs Specialist Cregg Group - Clare to requests from Regulators. Maintains an excellent understanding of the global medical device regulations especially with respect to Biocompatibility for example ISO 10993, and by identifying and critically 65000.0 26 days ago
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QA Supervisor - Day Shift Edwards Lifescience Ireland Ltd - Clare sensitivity Project management experience Proven expertise in Microsoft Office Suite with working knowledge of Enterprise Resource Planning (ERP) system, preferably JDE Experience working in a medical device 12000.0 26 days ago
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Quality Director Harmonics - Clare experience in the medical device industry or FDA-regulated environment. Proven experience in a senior leadership role (at least 5 to 7 years). In-depth knowledge of Quality Assurance and regulatory 27 days ago
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