In this role, the selected candidate will attend pre-booking and sales to operations turnover meetings to evaluate the accuracy of sales estimate and job layout. Reviews plans, specifications, and contract to determine project requirements.
In this role, you will work with all audiences to accelerate adoption of intel-based platforms, and document gaps/provide feedback to solution stakeholders, including: solution architects, vertical/horizontal business leaders, and partners.
As the Sr. Technical Support Specialist / Sys Admin you will be working in a highly visible role at a variety of client locations, working both independently and as part of a team to resolve a wide range of technical challenges.
In this role, you will be responsible for understanding the business use case and technical merits of storage and SSD based solutions, developing relationships with customer/partner decision-makers to influence the customers purchasing decision.
In this role, you will provide technical support via the infrastructure or application vendor to transform, implement, support and improve all corporate wide systems. Responsible for the monitoring, capacity planning, problem management oversight and protection of the production environment.
In this role, you will ensure the customer experience is at world class level for Corsair Products through the development and use of KPIs through all channels of customer interaction phone, chat and e-mails.
In this role, you will act as
learning & becoming proficient in new installations/ servicing the following products, but not limited to: CCURE 9000, Victor Video Edge, Genetech, Lenel On-guard, Prism, SiPASS & SiVeillance.
In this role, you will be expected to manage your business and be successful by challenging your customers and creating useful insights they can use to drive their research or product development forward.
As a dedicated Technical Specialist you will be responsible for reviewing the design dossiers of a wide range of Active Implantable Medical devices with the aim of determining whether the devices meet the requirements of the Active Implantable Medical Devices Directive and relevant harmonised standards.
In this role, you will evaluate complaints to determine whether an investigation is necessary and if Medical Device Reporting (MDR) is necessary in accordance with 21 CFR Part 803 Medical Device Reporting and 806 Corrections and Removals.