Senior Mechanical Engineer

ppChange people’s lives and love what you do Cochlear develops world-leading medical devices that help people hear. As a top 100 medical device company and market‑leader in implantable hearing devices, more people choose a Cochlear-branded cochlear implant system than any other. Our employees tell us that the number one reason they enjoy working for Cochlear is the opportunity to make a difference to people’s lives. /p pAre you passionate about solving complex engineering challenges that improve people’s lives? We are looking for an experienced bSenior Mechanical Engineer /b to lead the development of innovative active hearing implant technologies, surgical instruments, and packaging solutions from early‑stage concept through to devices ready for first‑in‑human and clinical research studies. /p pIn this role, you will play a key part in designing and delivering next‑generation implantable medical devices that transform hearing outcomes for recipients worldwide. Working within a multidisciplinary RD environment, you will combine technical expertise, creativity, and collaboration to develop safe, effective, and manufacturable solutions that meet the highest quality and regulatory standards. You will thrive in a dynamic environment, adapting effectively to evolving technical challenges, business priorities and project needs throughout the technology development process. /p h3What you will do /h3 h3Drive Mechanical Design Innovation /h3 ul lipLead the design and development of complex electro‑mechanical components for active hearing implant systems. /p /li lipTranslate user, clinical, manufacturing, and regulatory needs into robust engineering requirements. /p /li lipDefine, develop, and evaluate innovative concepts to solve challenging mechanical and surgical implementation problems. /p /li lipCollaborate with surgeons and clinical experts to optimize product usability and performance. /p /li lipConduct and facilitate engineering activities including concept generation, design reviews, risk analyses, DFMEA activities, simulations, and problem‑solving workshops. /p /li lipCreate and maintain high‑quality 3D CAD models, detailed drawings, and design documentation. /p /li lipCoordinate prototyping and supplier activities to support rapid product development. /p /li lipContribute to intellectual property development through patent disclosures and innovative technical solutions. /p /li /ul h3Lead Verification Validation Activities /h3 ul lipDevelop and execute verification and validation strategies to ensure device safety, effectiveness, and performance. /p /li lipDesign and implement test methods, fixtures, and protocols, including testing using temporal bone and cadaver models where appropriate. /p /li lipPrepare and review test plans, protocols, reports, and technical documentation. /p /li lipDrive continuous improvement of VV processes, methodologies, and best practices across the organization. /p /li lipSupport multidisciplinary engineering teams in planning and execution of development and testing activities. /p /li /ul h3Deliver High-Quality Medical Device Solutions /h3 ul lipEnsure compliance with quality management systems, regulatory requirements, risk management processes, and industry standards. /p /li lipProduce clear, accurate, and timely technical documentation. /p /li lipPartner with manufacturing teams to support prototype builds, product verification activities, and inspection planning. /p /li lipDrive design solutions that achieve strong manufacturability, reliability, and performance outcomes. /p /li lipDemonstrate agility and sound engineering judgement, adapting to changing technical requirements, emerging business priorities and evolving project contexts while maintaining focus on quality, compliance, and delivery objectives /p /li /ul h3Influence, Collaborate and Lead /h3 ul lipTake ownership of technical work packages and deliver project objectives within scope, schedule, and budget. /p /li lipCollaborate with cross‑functional teams including RD, Manufacturing, Quality, Regulatory Affairs, Clinical Affairs, and external suppliers. /p /li lipMentor junior engineers and students, sharing knowledge and promoting engineering excellence. /p /li lipContribute to the advancement of engineering practices, continuous improvement initiatives, and technology development programs. /p /li /ul h3What you’ll bring /h3 h3Essential Qualifications Experience /h3 ul lipMaster’s degree in Mechanical Engineering, Mechatronics, Biomedical Engineering, or a related discipline. (Master’s or PhD degree in a relevant scientific or engineering discipline (or equivalent). For candidates with degrees obtained outside Belgium, a formal recognition process may be required as part of the hiring journey. Support will be provided) /p /li lipMinimum b10 years’ experience /b in product design and development using 3D CAD tools. /p /li lipMinimum b5 years’ hands‑on experience /b in prototyping, testing, verification, a