Innovation/Design Control & Project Quality EngineerTeoxane SA • Geneva, Geneva, Switzerland

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Innovation/Design Control & Project Quality Engineer

Teoxane SA

Geneva, Geneva, Switzerland

Geneva, Geneva, Switzerland

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Control & Project Quality EngineerYou can find all of our job offers by clicking here: Teoxane were established in Geneva, Switzerland, inThey are specialized in the design and manufacturing of hyaluronic acid-based dermal fillers and dermocosmetics. Teoxane strength is to offer a global care. Using its products, practitioners can fill all kinds of wrinkles, from X to the deepest, to restore youthful volume X face, and to the neck and décolleté, with results. The strength of Teoxane is also its human size and independence. Teoxane has total freedom X , action and which makes the company the frame X growth of our business, we are looking for Control & Project Quality EngineerMain activitiesAct as QA throughout the product lifecycle, from X development to market post-market activities, and product withdrawal, including design change management.Perform X from X phase through completion of Design Transfer.Provide Quality support to Design Control stakeholders through daily support, coaching, and training to strengthen the Quality to the of Quality by Design (QbD) across R&D projects.Actively in design risk assessment activities, including risk and definition of risk and control responsible for the Design History File (DHF) management process, ensuring maintenance, and in line with change controls.Support compliance and continuous improvement of the Design Control process in accordance with ISOand 21 CFR 820, from X proper of processes, including Risk Management (ISO) and Human Factors/Usability (IEC), throughout all development in audits and inspections as a Subject Expert (SME), support Design & Development audit readiness, contribute to R&D process mapping and risk analyses, and support the Design Control training profileUniversity degree in Engineering or field.Minimum 7 years of professional experience in the Medical Devices or Pharmaceutical industry, including a minimum of 3 years in R&D Quality Assurance (Design).Strong knowledge of ISO, IEC, ISO, and 21 CFR 820, as well as requirements applicable to medical devices; experience with audits and inspections against these standards is required.Knowledge of Quality by Design (QbD).Fluent in English, French is an asset. jid6eab494aen jit0310aen jpiy26aen

Geneva, Geneva, Switzerland

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English

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