Senior NPI Manufacturing Engineer, Single Port Systems für Intuitive Surgical Sàrl in Port - myjob.ch
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      05.08.2026

      Senior NPI Manufacturing Engineer, Single Port Systems

      • Port
      • Festanstellung 100%

      • Merken
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      Intuitive Surgical Sàrl

      Intuitive Surgical Sàrl

      Senior NPI Manufacturing Engineer, Single Port Systems

      Career Opportunities

      Embeded Code End Code

      It started with a simple idea: what if surgery could be less invasive and recovery less painful? Nearly 30 years later, that question still fuels everything we do at . As a global leader in and , our technologies—like the and —have transformed how care is delivered for millions of patients worldwide

      robotic-assisted surgery

      We’re a team of engineers, clinicians, and innovators united by one purpose: to make surgery smarter, safer, and more human. Every day, our work helps care teams perform with greater precision and patients recover faster, improving outcomes around the world

      transform the future of healthcare

      Job Description

      • Contribute your technical skills in the areas of manufacturing process technologies, process development, early engagement with NPD, problem-solving, training, and project management in a growing medical device company. In this key role, you will be the driving force behind next generation product and process development within Ion Accessories
      • Primary Function of Position
      • Assist in developing and releasing manufacturing processes and EFTs for new accessories
      • Ensure processes meet quality standards. Manage and examine data for CPK and process capability, and implement improvements based on data
      • Conduct EFT qualifications to ensure readiness for production, validate equipment performance and reliability
      • Develop and validate test methods (TMV) to ensure product quality and compliance. Document and report validation results
      • Work closely with design engineers and clinical engineers to understand user needs and clinical requirements
      • Coordinate with quality and regulatory teams to ensure compliance with industry standards and regulations and support Supplier Engineering, Purchasing, Planning and Quality teams to resolve line facing issues
      • Resolve failures of varying complexity, of both process and hardware nature. Identify specific root cause and implement solutions to improve yield/manufacturability
      • Assist in product design reviews with a focus on DFX methods
      • Create and revise work instructions for assembly and test processes, and train manufacturing team on new content
      • Required Skills and Experience
      • Exceptional communication skills, both written and verbal. Necessary to engage with technicians, production management, product development, planning, purchasing, regulatory, inspection, customer support and clinical marketing organizations

      Arbeitsort: Port