Medical Device Compliance Specialist
2 weeks ago
**About the Role**
In this key role, you will provide regulatory direction to development project teams as a core team member and advise other functional units on the requirements in each target market.
You will review proposed labeling and instructions for use for compliance with applicable local and international regulations and recommend changes for labelling and internal documentation.
This is an excellent opportunity to become the Subject Matter Expert (SME) for the Biological safety process and work closely with Regulatory and Clinical Affairs to address biological aspects for submissions to EU/US regulators.
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Medical Device Compliance Manager
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Ennis, Clare, Ireland Cregg Group Full timeAbout the JobCregg Group is seeking an experienced Senior Regulatory Affairs Specialist to join our team.The Senior Regulatory Affairs Specialist will be responsible for developing and implementing regulatory strategies to support the timely and successful registration, approval, and maintenance of company and client products.This role requires strong...
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Medical Device Regulatory Expert
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Ennis, Clare, Ireland Cregg Group Full timeRole Overview:The Cregg Group is looking for a highly skilled Senior Regulatory Affairs Specialist to join its team. This is an exciting opportunity for a professional who wants to work in a dynamic and innovative environment and contribute to the success of the company.Key Responsibilities:Develop and implement regulatory strategies to support the...
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Medical Device Quality Assurance Specialist
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Ennis, Clare, Ireland Vitalograph Full timeVitalograph, a leading manufacturer of medical respiratory diagnostic devices, is seeking a highly skilled Medical Device Quality Assurance Specialist to provide quality assurance support and direction to operations and the QMS.The successful candidate will be responsible for documentation control, release of documents, updating bills of materials, and...
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Medical Device Tester
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Medical Device IT Technician
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Ennis, Clare, Ireland Vitalograph Full timeCompany Overview:Vitalograph is a renowned developer of medical respiratory diagnostic devices and software, dedicated to providing innovative solutions for healthcare professionals. With over 60 years of experience, we have established ourselves as a trusted partner in the industry.Our products are designed to help diagnose and treat respiratory disorders,...
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Global Regulatory Compliance Specialist
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Ennis, Clare, Ireland Cregg Group Full timeJob Summary:The Cregg Group is seeking a Senior Regulatory Affairs Specialist to join its team. This is a challenging and rewarding role that requires a high level of expertise in regulatory affairs and a passion for working in a fast-paced environment.Key Responsibilities:Develop and implement regulatory strategies to support the registration, approval, and...
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Ennis, Clare, Ireland Cregg Group Full timeResponsibilities:This is an excellent opportunity for a Testing and Validation Expert for Medical Devices to join Cregg Group's dynamic team. As a key member of the R&D department, you will be responsible for performing R&D testing, developing test methods, validating test results, and ensuring compliance with industry standards.You will work closely with...
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Senior Medical Device Software Developer
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Medical Device Assembly Specialist
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Ennis, Clare, Ireland Vitalograph Full timeCompany OverviewVitalograph is the world's leading manufacturer of medical respiratory diagnostic devices and software, used in the diagnosis of respiratory disorders. We design and manufacture respiratory diagnostic devices, software, and consumables for healthcare professionals.We serve customers in over 100 countries and have operations in Ireland,...
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Medical Device Firmware Engineer
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Ennis, Clare, Ireland Vitalograph Full timeVitalograph is a global company with operations in the UK, Ireland, Germany, and the USA. We are a dynamic and innovative organization, dedicated to improving patient outcomes through the development of cutting-edge medical devices and software.We are seeking an experienced Embedded Software Development Engineer to join our team in [location]. As a key...
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Medical Device Fabricator
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Medical Devices Quality Assurance Specialist
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Ennis, Clare, Ireland Vitalograph Full timeVitalograph is a world-leading manufacturer of medical respiratory diagnostic devices and software, serving customers in over 100 countries. Our products are used in the diagnosis of respiratory disorders and advanced high-reliability equipment systems for clinical drug trials.We design and manufacture respiratory diagnostic devices, software, and...
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Medical Device Testing Specialist
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Regulatory Affairs Specialist
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Ennis, Clare, Ireland Cregg Group Full timeRegulatory Affairs Specialist Excellent opportunity for a Senior Regulatory Affairs Specialist to join a thriving company in Co.Clare.The Senior Regulatory Affairs Specialist will be responsible for developing and implementing regulatory strategies to support the timely and successful registration, approval, and maintenance of company and client products.The...
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Senior Regulatory Specialist
1 week ago
Ennis, Clare, Ireland Cregg Group Full timeAbout the RoleWe are seeking an experienced Senior Regulatory Affairs Specialist to join our team at Cregg Group.The successful candidate will be responsible for providing regulatory support to the development project teams and ensuring compliance with applicable regulations.This role requires strong technical knowledge of medical device regulations,...
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Device Assembler
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Ennis, Clare, Ireland Edwards Lifescience Ireland Ltd Full timeCompany OverviewAt Edwards Lifesciences, our Manufacturing teams create the tools, technologies, and devices that transform patients' lives. Our facilities around the world are dedicated to making a meaningful difference in the lives of patients.Job DescriptionAs an Associate Assembler at Edwards Lifesciences, you will play a crucial role in applying skill...
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Quality Assurance and Compliance Engineer
1 week ago
Ennis, Clare, Ireland Vitalograph Full timeVitalograph, a global leader in medical respiratory diagnostic devices, seeks an experienced Quality Assurance and Compliance Engineer to support our operations and QMS.The successful candidate will be responsible for providing quality assurance support and direction to operations and the QMS, ensuring compliance with regulatory requirements. Key...
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Respiratory Device Assembly Specialist
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Medical Specialist Position
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Regulatory Affairs Expert
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Ennis, Clare, Ireland Cregg Group Full timeAbout Cregg GroupCregg Group is a thriving company in Co. Clare, offering an excellent opportunity for a Senior Regulatory Affairs Specialist to join our team.The Senior Regulatory Affairs Specialist will be responsible for developing and implementing regulatory strategies to support the timely and successful registration, approval, and maintenance of...