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Quality Systems Analyst 2 (f/m/x) 100% // Johnson & Johnson.

job details

summary.

  • Oberdorf, Basel-Landschaft
  • Temporary
  • 31. March 2025
  • specialism
    industry
  • contact
    Fabio Romano
  • reference number
    111362-20501

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job details

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.

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.

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FR

Fabio Romano

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