Sachbearbeiter Gebrauchsanweisungen// DepuySynthes in Zuchwil

veröffentlicht
Kontakt
Nadja Schuler, Randstad Inhouse Services J&J Zug
Jobtyp
Temporär
jetzt bewerben

job details

veröffentlicht
Ort
Zuchwil, Solothurn
Sektor
Administration
Jobtyp
Temporär
Referenznummer
138873-122
Kontakt
Nadja Schuler, Randstad Inhouse Services J&J Zug
Telefon
058 231 52 20
jetzt bewerben

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 265 operating companies in more than 60 countries employing approximately 127,100 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. Building on the legacy and strengths of two great companies, we are creating one organization that will be agile and better equipped in todays evolving health care environment. Our broad array of inspired, innovative and high-quality offerings help advance the health and wellbeing of people around the world.

Main resposibilities:
  • Responsible for processing OUS Instructions for Use (IFUs) DCO’s for Trauma, CMF, Spine and Power Tools franchises
  • DCO will be assigned to the IFU Coordinator in Agile with a Word document and formatted translated PDF of the final IFU’s.
  • Required to visually proof IFUs prior to releasing to production print using Docuproof software (training will be provided) for revisions to confirm approved Microsoft Word content has not been altered in final formatted IFU’s and all required language files are present.
  • Coordinate these activities with requesters – typically Marketing and Regulatory Affairs representative to support NPD launch timelines and milestones.
  • All activities should be performed ensuring compliance with defined procedures
  • Perform periodic review of procedures to verify accuracy, routing revisions in ADAPTIV for approval as needed

Qualifikation

Who we are looking for:

  • University/Bachelors Degree or Equivalent or completed KV
  • 2+ years professional experience with ability to prioritize work
  • Experience in a regulated medical industry preferred
  • High attention to detail
  • Experience with Agile PLM System is an asset
  • Comfortable working with minimal supervision while under tight timelines
  • Excellent organizational and communication skills
  • Fluent in English and German

This role based in Solothurn, Switzerland will initially be limited until the end of 2018, with an option for extension. 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!