Quality System Analyst // Johnson & Johnson in Neuchâtel

veröffentlicht
Kontakt
Andrea Oliveira, Randstad JnJ Neuchâtel Campus
Jobtyp
Mission d'intérim
jetzt bewerben

job details

veröffentlicht
Ort
Neuchâtel, Neuenburg
Sektor
Administration
Jobtyp
Mission d'intérim
Referenznummer
152865-49
Kontakt
Andrea Oliveira, Randstad JnJ Neuchâtel Campus
Telefon
032 934 90 38
jetzt bewerben

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.

We are looking for a:

Quality System Analyst 100%

temporary mission of 6 months

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.

Responsabilities:

  • The Quality Systems Analyst ensures the continuous education, implementation and improvement of Quality Systems and compliance with QS Regulation and ISO
  • The Quality Systems Analyst ensures that 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
  • 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 and 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

Qualifikation

  • Requires a minimum of 2 years related experience. Medical device manufacturing experience preferred.
  • University/Bachelor s Degree or Equivalent
  • Desirable Lean/Six Sigma Green Belt for this position, and also background in Statistics.
  • Able to communicate and writing skills in English
  • Mathematical and analytical thinking skills
  • Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations.
  • Ability to write reports, business correspondence, procedure manuals and related documentation that conform to prescribed style and format.
  • Ability to effectively present information and respond to questions from groups of managers, clients, and customers.

Location: Neuchâtel

Are you interested ? In this case, we are looking forward to receiving your complete application form (resume and work certificates).

! Only candidates available in very short deadlines and transmitted via our recruitment platform will be taken into consideration !