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Why Join Us?A career at BD means learning and working alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time.To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you’ll discover a culture in which you can learn, grow and thrive. And find satisfaction in doing your part to make the world a better place.Become a maker of possible with us!ResponsibilitiesSpecifying, reviewing, and revising methodologies and documentation for the fabrication of components, subassemblies, and final products. Identifying and driving continuous improvement activities in production.Improving current and developing new equipment and manufacturing aides as well as defining / updating / documenting production procedures. Providing technical guidance and liaison to R&D and QE and executing process characterization (i.e., via DoE, Ishikawa, etc.) and process capability analysisProviding consistent support to production lines, the development of new products and processes, and their transfer into production. Resolve equipment issues and respond to operator questions. Collaborate with both internal (BD Wangs & Corporate) and external parties on all aspects of production processes.Managing, performing and documenting of process validations and support of Test Method Validations (TMV)Process monitoring, data compilation and reporting as well as failure analysis (RCAs etc.)Leading and executing maintenance, repair, and revalidation workDocumenting all activities according to the relevant regulatory and stringent company standardsPreferred Requirements:University Degree in engineering or equivalent.Professional experience in medical technology, materials science, and mechanical engineering.Proven track record in the field of medical device engineering of at least 3 years.Industry experience in the manufacturing or prototyping of medical devices (preferably catheters or comparable).Experienced producing in a regulated environment (ISO 13485, 14971) in addition to FDA regulations.Preferred: Proven track record regarding Lean manufacturing. Strong background regarding Six Sigma philosophy.Fluency in both German and English languagesClick on apply if this sounds like you!Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.To learn more about BD visit:https://bd.com/careersRequired SkillsOptional Skills.Primary Work LocationCHE Wangs - StraubstrasseAdditional LocationsWork Shift
