Quality Engineer // Johnson & Johnson in Selzach

veröffentlicht
Kontakt
Stefanie Aerni, Randstad Inhouse Services Johnson&Johnson Zuchwil
Jobtyp
Temporär
jetzt bewerben

job details

veröffentlicht
Ort
Selzach, Solothurn
Sektor
Administration
Jobtyp
Temporär
Referenznummer
139322-108
Kontakt
Stefanie Aerni, Randstad Inhouse Services Johnson&Johnson Zuchwil
Telefon
058 231 36 15

Stellenbeschreibung

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

Qualifikation

Who we are looking for

  • Bachelor's degree, preferably in engineering or in a related technical field or equivalent experience
  • 3-5 years of general work experience
  • Knowledge of product / process risk management (FDA and ISO standards)
  • Experience with statistics, lean and Six Sigma methods, including measurement systems analysis, SPC, DOEs, reliability, etc.
  • 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
  • Very good command of English and German

This job based in Selzach, Switzerland will initially be limited to approx. 6 months. 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!