Senior QS Analyst
Johnson & Johnson Services, Inc
Le Locle, Switzerland
vor 7 Tg.

Job Description

Caring for the world oneperson at a time inspires and unites the people of Johnson &Johnson. This culture of caring is the focus of our corporate philosophy, thatare anchored in the internationally applicable Credo.

DePuySynthes Companies of Johnson& Johnson is the largest, most comprehensive orthopedic and neurologicalbusiness in the world.

DePuy Synthes offer an unparalleled breadth and depth oftechnology, devices, services and programs in the areas of jointreconstruction, trauma, spine, sports medicine, neurological,cranio-

maxillofacial, power tools and biomaterials. Ourbroad array of inspired, innovative and high-quality offerings, help advancethe health and wellbeing of people around the world.

For our production site, weare looking for a highly committed : Senior QS Analyst basedin Le Locle (Permanent) Further responsibilities and duties are Ensuresconsistent and correct execution of change management procedures at the site tomaintain the quality and compliance of the process and the records for documentcreation and changes.

This includes : Review site change request and change order documentationProvide guidance / training on Document management toolsand requirementsAssist users with documentation, actions andjustificationsAssist with selection of assessment owners and approversDrives timelyand compliant execution of document changes by driving cross-

collaborationacross functions, monitoring progress, and elevating issues in a timely mannerfor resolution.Generate andmonitor Document management performance indicator.

If necessary, implement actionsfor performance improvement.Identifiessite needs to meet and improve system performance of document control at thesite level and escalates to appropriate representative and management in atimely manner.

Supports theDocument Control process initiatives impacting the site (ei : local procedureupdate, document translation, cross-

operating companies harmonization andprocess streamlining) and ensure continuity of the application of processes andsystems at site level.

  • Assists inimplementing document control systems and procedures.Supportscompliance activities by participating in audit readiness;
  • assisting inInternal and External audits; serving as Subject Matter Expert back-up forDocument and Change Control process during audits;
  • supporting theinvestigation, response, and remediation of site-specific QS audit observations.Complaints management : record, follow-

    up, investigation, correctiveaction initiation, direct contact with distributors / affiliates / customers.Manage RecordManagement process and act as SME.

    QualificationsUniversity / Bachelor’s Degree or Equivalent.Fluent in French and in English.Knowledge / experience of medical or technical industry.

    Previous experience in Quality System.Ability to communicate at different levels of the organization, and to interact with and influence cross-

    functional and cross-business teams to drive results (negotiation skills).Conscientious / Rigorous / Analytical Mind.Well organized and systematic approach.

    Knowledge of Microsoft Office tools. If you want to be a change agent in a challengingenvironment and shape the future quality organization, please send us youronline application (CV, Motivation Letter, Working References etc.

    Primary LocationSwitzerland-Neuchâtel-Le Locle-OrganizationMedos International Sarl (7898)Job FunctionQuality SystemsRequisition ID1905742789W

    Caring for the world oneperson at a time inspires and unites the people of Johnson &Johnson. This culture of caring is the focus of our corporate philosophy, thatare anchored in the internationally applicable Credo.

    DePuySynthes Companies of Johnson& Johnson is the largest, most comprehensive orthopedic and neurologicalbusiness in the world.

    DePuy Synthes offer an unparalleled breadth and depth oftechnology, devices, services and programs in the areas of jointreconstruction, trauma, spine, sports medicine, neurological,cranio-

    maxillofacial, power tools and biomaterials. Ourbroad array of inspired, innovative and high-quality offerings, help advancethe health and wellbeing of people around the world.

    For our production site, weare looking for a highly committed :

    Senior QS Analyst basedin Le Locle

  • Ensuresconsistent and correct execution of change management procedures at the site tomaintain the quality and compliance of the process and the records for documentcreation and changes. This includes :
  • Drives timelyand compliant execution of document changes by driving cross-collaborationacross functions, monitoring progress, and elevating issues in a timely mannerfor resolution.
  • Generate andmonitor Document management performance indicator. If necessary, implement actionsfor performance improvement.
  • Identifiessite needs to meet and improve system performance of document control at thesite level and escalates to appropriate representative and management in atimely manner.
  • Supports theDocument Control process initiatives impacting the site (ei : local procedureupdate, document translation, cross-
  • operating companies harmonization andprocess streamlining) and ensure continuity of the application of processes andsystems at site level.

  • Assists inimplementing document control systems and procedures.
  • Supportscompliance activities by participating in audit readiness; assisting inInternal and External audits; serving as Subject Matter Expert back-
  • up forDocument and Change Control process during audits; supporting theinvestigation, response, and remediation of site-specific QS audit observations.

  • Complaints management : record, follow-up, investigation, correctiveaction initiation, direct contact with distributors / affiliates / customers.
  • Manage RecordManagement process and act as SME.
  • University / Bachelor’s Degree or Equivalent.
  • Fluent in French and in English.
  • Knowledge / experience of medical or technical industry.
  • Previous experience in Quality System.
  • Ability to communicate at different levels of the organization, and to interact with and influence cross-functional and cross-
  • business teams to drive results (negotiation skills).

  • Conscientious / Rigorous / Analytical Mind.
  • Well organized and systematic approach.
  • Knowledge of Microsoft Office tools.
  • If you want to be a change agent in a challengingenvironment and shape the future quality organization, please send us youronline application (CV, Motivation Letter, Working References etc.).

    Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

    Equal Employment Opportunity PostersIf you are an individual with a disability and would like to request a reasonable accommodation as part of the employment selection process, please complete the form below.

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    Contact Us with any questions or search this site for more information.

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