Design Assurance Engineer, Device Technical Operations ( 18 Months FTC )

Design Assurance Engineer, Device Technical Operations ( 18 Months FTC )Aplikujlocations: Northern Cross, Dublin, Irelandtime type: Praca na pełny etatposted on: Opublikowano dzisiajjob requisition id: RMcDermott Laboratories LimitedViatris to globalna firma medyczna, która jest wyjątkowo pozycjonowana, by zniwelować tradycyjne podziały między lekami generycznymi a markami, łącząc najlepsze z obu, aby bardziej kompleksowo odpowiadać na potrzeby zdrowotne na całym świecie. Z misją umożliwienia ludziom na całym świecie zdrowszego życia na każdym etapie życia, zapewniamy dostęp na dużą skalę, obecnie dostarczając wysokiej jakości leki około miliardowi pacjentów rocznie i dotykając wszystkich momentów życia - od narodzin po koniec życia, od ostrych schorzeń po choroby przewlekłe. Zostaliśmy uwzględnieni na wielu listachnagród, które pokazują wpływ, jaki wywieramy. Every day, we rise to the challenge to make a difference and here's how the Design Assurance Engineer, Device Technical Operations role will make an impact:Key responsibilities for this role include: Provide Design Assurance oversight and support to the creation and maintenance of Technical Documentation supporting development and on-market combination products / medical devices. Provide Design Assurance oversight for the transfer of manufacturing of Devices and Combination Products from the Global Device Development (GDD) Group in R&D to commercial manufacturing sites as per the GDD design control process in compliance with ISO 13485 and 21 CFR 820. Manage, review, and approve change controls issued from the commercial site or from GDD which are deemed to impact the device/combination product. Provide Design Assurance support on site as required at suppliers or manufacturing sites for device-related complaints, support device-related investigations to root cause and the establishment of appropriate corrective actions. The minimum qualifications for this role are: Degree in Engineering/Science Previous experience of Design Assurance in device development or high volume GMP manufacturing environment for devices and/or combination products. Experience authoring technical reports and producing high quality documentation within a regulatory controlled GMP environment. Experience in quality management, ideally in the medical device industry or another regulated environment A working knowledge of MDR 2017/745, ISO 14971, ISO 13485 & FDA 21 CFR Part 820 Design Control requirements, would be an advantage. It is essential that the candidate will be both highly innovative and well organized, having excellent planning and communication skills and able to operate across all site teams. The candidate must be able to work under pressure and have a proven track record of problem solving and effective time management. Willingness to travel as necessary between the Global Device Development Teams, Affiliates & suppliers.At Viatris, we offer competitive salaries, benefits, and an inclusive environment where you can use your experiences, perspectives, and skills to help make an impact on the lives of others.W Viatris stawiamy sobie za cel by zaoferować Ci konkurencyjne wynagrodzenie, świetne benefity i wspierające środowisko pracy, gdzie będziesz mógł rozwijać swoje doświadczenie, umiejętności i osiągać nowe cele, mając wpływ na zdrowie innych.