Senior Expert Engineering – Assembly for Medical Device

vor 2 Wochen


Basel, Schweiz Healthcare Businesswomen’s Association Vollzeit

Job Description SummaryLocation: Basel, SwitzerlandAt Novartis, we are reimagining medicine to improve and extend people's lives. We discover and develop breakthrough treatments and find new ways to bring cures to as many people as possible. Without safe, easy-to-use, high-quality drug delivery systems our patients could not get their medicines. This is where you come in; the Device Technology Solution Center needs you as Senior Expert Engineering for the development of drug device combination products working alongside our talented, bright and diverse teams. Our Device Technology Solution Center drives the technical development of auto-injectors as well as novel drug delivery principles, e.g. drug delivery to the brain or radioligand therapy. We closely collaborate with project management, human factors engineers, packaging experts, analytical testing, production, external partners, experts and many more. The aim is to develop and or integrate innovative drug delivery systems with drug formulation and author state-of-the-art technical documentation for health authorities and production.ResponsibilitiesDevelop platforms and collaborate with cross-functional teams to deliver safe, user-friendly, and reliable productsLead and support teams in the field of assembly for parts/device, design equipment and process across from prototyping to commercial scaleCreate and maintain relevant Design History File (DHF) documents, ensuring high-quality device design and developmentContribute to all phases of medical device development: ideation, prototyping, piloting, and manufacturing transferEnsure components meet quality standards for clinical trials and commercial productionCollaborate with external partners, including prototypers, toolmakers, and CMOsIdentify root causes of issues, define and implement robust solutionsRole RequirementsDegree in mechanical engineering or equivalentPreferably 5 years of experience in medical device developmentProficient spoken communication and excellent technical writing skills in EnglishProven experience in assembly of plastic and metal components / sub-assembliesProven experience in design for manufacturing and design for assemblyGood knowledge in key regulations and standards (e.g. ISO 13485, ISO 23908, ISO 11608, ISO 10993, MDR, Design Controls)Ability to interact with cross functional team in matrix organizationMinimum 80% on site work – 4 days/weekTravels to visit suppliers and CMOsCommitment to Diversity & InclusionNovartis is committed to building an outstanding, inclusive work environment and diverse teams’ representative of the patients and communities we serve.Skills Desired #J-18808-Ljbffr



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