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
Life Sciences
Jobtyp
Temporär
Referenznummer
126210-27
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. This culture of caring is the focus of our corporate philosophy, that is anchored in the internationally applicable Credo. 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 134,000 people. Our worldwide headquarters is in New Brunswick, New Jersey, USA.

ETHICON Neuchâtel is responsible for the production of implants for the treatment of female incontinence and bio-resorption products to stop bleeding during surgical procedures.

Quality Systems Analyst will work within the Quality Systems Department which resides under the Quality Operations structure that reports to the Plant QA Manager. Quality Systems Department is responsible to maintain the high-quality standards of the product manufacturing process and compliance with regulatory requirements.

Responsibilities :

Under the Quality Systems Department and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:
  • The Quality Systems Analyst ensures the continuous education, implementation and improvement of Quality Systems and compliance with QS Regulation and ISO within the Ethicon Sarl facility.
  • The Quality Systems Analyst ensures that the Ethicon Sarl, Document Control and Change Control Processes and structure meet all business and regulatory requirements.
  • Responsible for the Site Records Management being the Site Record Management representative for Ethicon Sarl.
  • 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.
  • Determines root causes of quality issues and develops corrective actions and recommendations.
  • Suggests process changes when appropriate.
  • 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
  • For those who supervise or manage a staff, responsible for ensuring that subordinates 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

Who we are looking for :

  • University/Bachelor's Degree or Equivalent or commercial CFC woth experience in a quality departement.
  • Requires 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. 7 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!