QS Analyst // Johnson & Johnson

Job content

Jobdescription

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.
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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!