Doc Management Change Analyst // DepuySynthes in Zuchwil

veröffentlicht:
Ort
Zuchwil, Solothurn
Sektor
Life Sciences
Jobtyp
Temporär
Referenznummer
138873-114
Kontakt
Nadja Schuler, Randstad JnJ HQ
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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 127,000 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. With a focus on activating insights to develop innovative, comprehensive solutions, we are inspired to advance patient care in greater ways than either company could accomplish on its own.

Main Responsibilities:

The Document Management Change Analyst will be accountable for the administration of the Change Order (CO) process. He/she will be accountable for compliance with the regulatory and compliance requirements as it pertains to Documentation and Documentation Management. This individual will be responsible for the timely processing and release of new and changed controlled documents.



  • Controlling and release of change requests
  • Release of change orders
  • Support the end users in creation of changes
  • Support the end users in handling of the office application (Word, Excel)

Qualifikation


  • University or FH degree or equivalent
  • 1 - 2 years work experience in a GMP and/or ISO regulated environment
  • Previous document management experience
  • Proficient with various PLM (Product Lifecycle Management)
  • Advanced knowledge of MS-Office, Systems such as Agile is preferred
  • Customer service oriented with good communication skills
  • Detail oriented with ability to troubleshoot
  • Fluent in written and spoken German & English

This role based in Zuchwil, Switzerland will initially be limited to 12 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 by email to nadja.schuler@ch.randstad.com. Or give us a call if you have any questions!

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