Quality Engineer (f/m/x) 50%-100% // Johnson & Johnson in Oberdorf

Caring for the world, one person at a time... inspires and unites the people of Johnson & Johnson. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world. We have more than 260 operating companies in more than 60 countries employing approximately 134,000 people. Our worldwide headquarters is in New Brunswick, New Jersey, USA.

DePuy Synthes Companies of Johnson & Johnson is the largest, most comprehensive orthopedic and neurological business in the world. DePuy Synthes offer an unparalleled breadth and depth of technology, devices, services and programs in the areas of joint reconstruction, trauma, spine, sports medicine, neurological, cranio-maxillofacial, power tools and biomaterials. Our broad array of inspired, innovative and high-quality offerings, help advance the health and wellbeing of people around the world.

Main Responsibilities

• Support of quality improvement initiatives for the continuous improvement of processes
• Planning and implementation of validation activities
• Monitoring of processes, collecting, checking and evaluating data
• Planning and implementation of product / process controls
• Collecting data and performing various analytical / statistical analyzes and interpretations as part of process optimization and day-to-day operations
• Support with internal and external audits

Who we are looking for

• Bachelor's degree, preferably in engineering or in a related technical field or equivalent experience
• Knowledge of statistics, lean and Six Sigma methods, including measurement systems analysis, SPC, DOEs, reliability, etc. is a plus
• Knowledge of the application of statistical software (LIMS) is preferred
• A good technical understanding of manufacturing facilities and processes
• A basic understanding of GMP / ISO regulations and validation regulations
• Experience working in an FDA and European regulatory environment preferred
• Very good command of English and German

This job based in Oberdorf BL, Switzerland is available immediately and will initially be limited to 31.12.2022. If you are interested in working for a global leading health care company in a challenging role, then send us your application in English today. Or give us a call if you have any questions!