
Technical Device Implementation Specialist
2 days ago
Job Title: Technical Support Specialist
Job DescriptionAs a technical support specialist, you will be responsible for providing assistance to users during the implementation of new devices. Your primary goal will be to ensure a seamless transition by addressing any refresh issues that may arise.
Key Responsibilities:- Address device refreshes in the order specified on a provided sheet.
- Disconnect and remove hardware, placing it on a designated trolley or area for later transport to the storage room.
- Record removed Asset details on laptops according to agreed documents.
- Place new devices and connect them to monitors, power, LAN connections, and other necessary components.
- Record new Asset details on laptops according to agreed documents.
- Power up new devices, enter BIOS settings, and perform checks as documented by the HCLTech team.
- Ask users to log on and begin Auto-pilot reimaging from provided instructions. Assist if users struggle to start Auto-Pilot.
- Revisit each user to check progress and determine if intervention is required.
- Take removed old devices to the storeroom area and stack them in designated locations.
- Send pre-agreed closure sheets with status updates.
For this role, you should have strong technical skills, excellent communication abilities, and a patient demeanor.
BenefitsThis position offers a unique opportunity to work with cutting-edge technology and develop your technical expertise.
OthersDuring the 5-day Hypercare period, you will be expected to re-attend calls for refresh if issues arise.
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Dublin, Dublin City, Ireland Viatris Inc. Full timePrincipal Device Technical Regulatory Specialist page is loadedPrincipal Device Technical Regulatory SpecialistApply locations Northern Cross, Dublin, Ireland time type Full time posted on Posted Today job requisition id R McDermott Laboratories LimitedAt VIATRIS, we see healthcare not as it is but as it should be.We act courageously and are uniquely...
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Device Technical Regulatory Associate Specialist
3 weeks ago
Dublin, Dublin City, Ireland Viatris Full timeSocial network you want to login/join with:Device Technical Regulatory Associate Specialist, Dublincol-narrow-leftClient:ViatrisLocation:Dublin, IrelandJob Category:Other-EU work permit required:Yescol-narrow-rightJob Reference:07c2a9724d21Job Views:6Posted:19.08.2025Expiry Date:03.10.2025col-wideJob Description:At VIATRIS, we see healthcare not as it is but...
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Dublin, Dublin City, Ireland Viatris Inc. Full timePrincipal Device Technical Regulatory Specialist page is loadedPrincipal Device Technical Regulatory SpecialistApply locations Northern Cross, Dublin, Ireland time type Full time posted on Posted Today job requisition id R5660652 McDermott Laboratories LimitedAt VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely...
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Medical Device Innovation Specialist
1 day ago
Dublin, Dublin City, Ireland beBeeQuality Full timeJob Title: Senior Physicist/Clinical EngineerOur organization is seeking an experienced medical device technical specialist to lead the design and implementation of a Quality Management System (QMS) aligned to ISO13485.Key Responsibilities:Design and implement a QMS that supports the max fax prosthetic service at the hospital.Develop a framework for...
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Prosthetic Service Technical Specialist
1 day ago
Dublin, Dublin City, Ireland beBeeMedical Full time €75,000 - €105,000Job DescriptionWe are seeking a highly skilled medical device technical specialist to lead the design and implementation of a Quality Management System (QMS) aligned to ISO13485 standards. The QMS will support the max fax prosthetic service at the hospital and provide a framework for continual innovation.
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Technical Support Specialist
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Medical Device Regulatory Expert
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Dublin, Dublin City, Ireland beBeeRegulatory Full time €80,000 - €120,000Regulatory Affairs Specialist RoleThe position of Regulatory Affairs Specialist is responsible for overseeing post-market activities for medical devices, supporting regulatory processes and procedures, authoring and reviewing regulatory documentation, and ensuring timely and high-quality execution of all deliverables.Key Responsibilities:Develop and...