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.
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
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!