Quality Systems Analyst 2

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 120,000 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:In this position you support compliance and continuous improvement of the Quality System (QS) for the Oberdorf site. Main responsibilities shall include:

• Have oversight and support the tracking of QS metrics at site level. Communicate status and issues to stakeholders and management, as needed.
• Review and ensure effective completion of Nonconformances (NC), Corrective and Preventive Action (CAPA), and Internal Audit (IA) Observations.
• Support site Document Control and Records Information Management activities.
• Support the coordination, preparation, facilitation, execution, and tracking of activities of the Quality Progress Review (QPR), Quality System Management Review (QSMR), and other KPI metrics meetings.
• Provide guidance on requirements of QS processes to resources that execute these processes.
• May be requested to participate in audit readiness activities, as well as assist with the preparation and execution of Internal and External Audits.
  

  Qualifikationen

  Who we are looking for:

  • University/Bachelor's Degree or Equivalent preferred (e.g., Technical Qualification with Further Education)
  • Experience in Medical Devices; Experience with DPS/J&J highly preferred
  • Experience in Technical writing is a plus
  • Project management experience is a plus
  • Experience in training/coaching others on requirements of procedures is a plus
  • Strong knowledge of Microsoft PowerPoint, Word, SharePoint, and Teams required
  • Detail-oriented and accurate
  • Time-oriented (i.e., able to recognize and adhere to strict timelines)
  • Strong communication and interpersonal skills (collaboration with multiple stakeholders is required)
  • Ability to follow-up with management-level stakeholders, and challenge, as necessary to ensure compliance to procedural requirements
  • German language skills highly preferred

    This job based in Oberdorf BL, Switzerland will initially be limited to a 9-month contract. 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