QS Analyst // Johnson & Johnson in Neuchâtel

veröffentlicht
Kontakt
Andrea Oliveira, Randstad Inhouse Services Johnson&Johnson Neuchâtel Campus
Jobtyp
Temporär
jetzt bewerben

job details

veröffentlicht
Ort
Neuchâtel, Neuenburg
Sektor
Administration
Jobtyp
Temporär
Referenznummer
136704-74
Kontakt
Andrea Oliveira, Randstad Inhouse Services Johnson&Johnson Neuchâtel Campus
Telefon
032 934 90 38

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.

Johnson & Johnson is looking for their futur : Quality System Analyst for Neuchâtel

Responsibilities

  • The Quality Systems Analyst ensures the continuous education, implementation and improvement of Quality Systems and compliance with QS Regulation within the Medos Sarl (Mitek Division) facility.
  • The Quality Systems Analyst ensures that the Medos Sarl (Mitek Division), Document Control and Change Control Processes and structure meet all business and regulatory requirements.
  • Lead the implementation and administration of quality management systems in accordance with applicable standards.
  • Ensures quality systems are effectively deployed. / Performs periodic checks to verify appropriate application.
  • Maintain regular interface with Management:
    • To assist in the development of Quality Metrics.
    • To achieve company's Quality goals.
  • Uses statistical methods, quality tools and computer-generated reports to continuously improve process capability.
  • Provide education/training as needed regarding Document Control and Change Control processes including MVI/Validation Documents.
  • Leads and participates in quality system improvement initiatives. / Suggests process changes when appropriate.
  • Determines root causes of quality issues and develops corrective actions and recommendations.
  • Establishes, maintains and implements communications to increase awareness and promote improvement of quality issues across the business.
  • Assists with external audits, generating reports with corrective action plans and ensuring implementation of corrective actions in a timely manner.
  • Backup on other tasks within QS department to assure business continuity, if required.
  • Responsible for communicating business related issues or opportunities to next management level.
  • Follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicable.
  • Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures.
  • Performs other duties assigned as needed.

Qualifikation

Requirements

  • University/Bachelor's Degree or Equivalent / Commercial CFC with experience in quality departement
  • Requires up to a minimum of 2 years related experience. Medical device manufacturing experience preferred.
  • Desirable Lean/Six Sigma Green Belt for this position and background in Statistics.
  • Able to communicate and writing skills in English
  • Mathematical and analytical thinking skills

This role based in Neuchâtel, Switzerland will initially be limited to approx. 18 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 or French today. Or give us a call if you have any questions!