regulatory affairs specialist // depuysynthes in Zuchwil

Nadja Schuler, Randstad Inhouse Services J&J Zug
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job details

zuchwil, solothurn
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nadja schuler, randstad inhouse services j&j zug
058 231 52 20
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job description

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 130,000 people. Our worldwide headquarters is in New Brunswick, New Jersey, USA.

DePuySynthes Companies of Johnson & Johnson is the largest, most innovative and comprehensive orthopaedic and neurological business in the world. DePuySynthes Companies will offer an unparalleled breadth and depth of products, services and programs in the areas of joint reconstruction, trauma, spine, sports medicine, neurological, craniomaxillofacial, 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 today´s evolving health care environment.

Main Responsibilities:

  • Providing support for Wave 2b and 3 market registrations and license renewals
  • Providing documentation to support international registration and tender requests
  • Preparing responses to questions and requests from health authorities for product registrations
  • Submission of requests for Certificates of Free Sale, legalization and notarization of documents
  • Ensuring compliance with regulatory agency regulations and interpretations
  • Providing solutions to a variety of problems of moderate scope of complexity
  • Maintaining and archiving all regulatory documentation


Who we are looking for:

  • Work experience in a highly-regulated environment is a major plus
  • Knowledge of Medical Device regulations and registration requirements would be an asset
  • Ability to work both independently and in a team environment
  • Ability to problem solve, recognize and find solutions for gaps in processes
  • Excellent skills in computer software such as MS Word, Excel, PowerPoint
  • Strong organizational skills
  • Ability to communicate clearly
  • Excellent English spoken and written, German is an asset

This role based in Solothurn, Switzerland will initially be limited to approx. 12 months. If you are interested in working for a global leading health care company in a challenging role, then use this entry level position and send us your application in English today. Or give us a call if you have any questions!