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Search Results for Lead Quality Engineer
| Job Title. | Location | Salary | Actions |
Design Assurance EngineerJob title: Design Assurance Engineer Location: Parkmore Business Park, Galway (Hybrid working 2 days a week on site) Benefits: Competitive salary, 10% bonus, Hybrid working, Full family healthcare, flexible working hours and pension contribution. Also an excellent opportunity to build your career with an exciting Medical Device company going through a growth phase. Company: My client are a rapidly growing medical device company offering a highly differentiated solution in SFA interventions. Their culture of innovation helps each individual develop...Location: Clare, Galway, Galway City, Limerick, Limerick City, |
EU | Not Disclosed | |
Reg Affairs SpecialistRole: Regulatory Affairs Engineer Location: Parkmore, Galway (Hybrid working) Benefits: Top salary Company: My client are a growing Medical Device company who have recently moved into a high tech new site in Parkmore. They have developed an innovative new technology to improve the performance of Vascular stents. Role: Reporting to the Senior Regulatory Affairs Manager, as a Regulatory Affairs Specialist you will play a key a key role in the implementation of post-market activities within Veryan. This is a ...Location: Connaught, Galway, Galway City, Leitrim, Limerick, |
EU | Not Disclosed | |
Design Assurance EngineerJob title: Design Assurance Engineer Location: Parkmore Business Park, Galway (Hybrid working 2 days a week on site) Benefits: Competitive salary, 10% bonus, Hybrid working, Full family healthcare, flexible working hours and pension contribution. Also an excellent opportunity to build your career with an exciting Medical Device company going through a growth phase. Company: My client are a rapidly growing medical device company offering a highly differentiated solution in SFA interventions. Their culture of innovation helps each individual develop...Location: Clare, Galway, Galway City, Limerick, Limerick City, |
EU | Not Disclosed | |
Project Manager Design AssuranceJob title: Design Assurance Program Manager Location: Ballybrit Upper Industrial Estate, Galway Benefits: Hourly rate contract, 3 days a week (Partime), Hybrid working Company: My client are a global leader in the medical device industry and expert in the design, development, and manufacturing of complex medical devices and component technologies. Responsibilities: • Lead Quality Representative on projects, directly contributing and/or providing guidance to others to establish appropriate Design History File / Device Master Record docume...Location: Galway, Galway City, |
Galway | Not Disclosed | |
Project Manager Design AssuranceJob title: Design Assurance Program Manager Location: Ballybrit Upper Industrial Estate, Galway Benefits: Hourly rate contract, 3 days a week (Partime), Hybrid working Company: My client are a global leader in the medical device industry and expert in the design, development, and manufacturing of complex medical devices and component technologies. Responsibilities: • Lead Quality Representative on projects, directly contributing and/or providing guidance to others to establish appropriate Design History File / Device Master Record docume...Location: Galway, Galway City, |
Galway | Not Disclosed | |
Quality EngineerJob title : Quality Engineer Location: Galway Business Park, Dangan Benefits: Competitive salary, 10% bonus, Share options, excellent opportunity to develop your experience and career in an exciting start up helping develop a product from its very early stages. Company: My client an early-stage medical device start-up company focused on the design and development of novel devices for the treatment of Intracranial Atherosclerotic Disease. This is a new and evolving treatment area likely to be the next frontier in Neuro-intervention. ...Location: Galway, Galway City, |
Galway | Not Disclosed | |
Design Assurance Program ManagerJob title: Design Assurance Program Manager Location: Ballybrit Upper Industrial Estate, Galway Benefits: Hourly rate contract, 3 days a week (Partime), Hybrid working Company: My client are a global leader in the medical device industry and expert in the design, development, and manufacturing of complex medical devices and component technologies. Responsibilities: • Lead Quality Representative on projects, directly contributing and/or providing guidance to others to establish appropriate Design History File / Device Master Record docume...Location: Galway, Galway City, |
Galway | Not Disclosed | |
Design Assurance Program ManagerJob title: Design Assurance Program Manager Location: Ballybrit Upper Industrial Estate, Galway Benefits: Hourly rate contract, 3 days a week (Partime), Hybrid working Company: My client are a global leader in the medical device industry and expert in the design, development, and manufacturing of complex medical devices and component technologies. Responsibilities: • Lead Quality Representative on projects, directly contributing and/or providing guidance to others to establish appropriate Design History File / Device Master Record docume...Location: Galway, Galway City, |
Galway | Not Disclosed | |
Quality SpecialistJob title: Quality Assurance Specialist Location: Western Business Park, Shannon, Co. Clare Benefits: Good salary, Healthcare, pension, 25 days holidays, opportunity to grow your career with exciting Medical Device company working on projects from concept. Summary: The Quality Systems specialist role will involve supporting the development and implementation of the Quality Management System with my Medical Device client in order to maintain 2017/745(MDR), ISO 13485, ISO 14971, ISO 9001 and FDA QSR standards and requirements. The QMS includes m...Location: Clare, Limerick, Limerick City, Republic of Ireland, |
EU | Not Disclosed | |
Quality SpecialistJob title: Quality Assurance Specialist Location: Western Business Park, Shannon, Co. Clare Benefits: Good salary, Healthcare, pension, 25 days holidays, opportunity to grow your career with exciting Medical Device company working on projects from concept. Summary: The Quality Systems specialist role will involve supporting the development and implementation of the Quality Management System with my Medical Device client in order to maintain 2017/745(MDR), ISO 13485, ISO 14971, ISO 9001 and FDA QSR standards and requirements. The QMS includes m... |