> Markdown version of [/jobs/ext/4650776-expert-engineering-device-development](https://www.wearedevelopers.com/jobs/ext/4650776-expert-engineering-device-development). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Expert Engineering Device Development - **Company:** Novartis - **Location:** Langkampfen, Austria - **Experience:** Expert - **Salary:** €66,918 - €117,800 - **Contract:** Permanent contract - **Skills:** Systems Integration, Communication Devices - **Published:** November 10, 2026 - **Apply:** https://novartis.wd3.myworkdayjobs.com/en-US/Novartis_Careers/job/Schaftenau/Senior-Expert-Engineering-Device-Development_REQ-10074221-2 ## About the Role * Bachelor, Master or PhD degree in engineering or equivalent. * Preferably 5+ years of experience working in development of medical device and/or combination products; preferred in pharmaceutical area or similar. * Experience in developing plastic and metal components; tolerance analysis, modelling and testing. * Excellent skills in English, verbal and written. German language skills are of advantage. * Autonomous and independent working style with interest to work in medical device development and life cycle management projects. * Ability to interact with cross functional team in matrix organization. ## Description * Deliver technical development and life-cycle management in cross-functional teams for easy-to-use, safe and robust products. * Responsible for device constituent parts of an autoinjector, the system integration of prefilled syringes together with the autoinjector into a combination product and timely delivery of technical aspects of one or more projects as well as LCM of commercial products. * Support device design development following the design control process and applicable regulatory framework. * Ensure components are delivered and controlled to the required quality for clinical trials and commercial production. * Support internal & external audits on medical devices related matters and provide input to health authority questions.