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2 Auditor Stellen in Neuenburg gefunden

Auditor Jobs in Neuenburg

Bei einem Auditor handelt es sich um einen Unternehmensberater. Da Auditoren sowohl bei Wirtschaftsprüfungsgesellschaften als auch bei anderen grossen Unternehmen in Wirtschaft, Technik und Industrie tätig sein können, unterscheidet man zwischen externem und internem Auditor. In beiden Fällen führt der Auditor Audits durch: Er analysiert die Rentabilität von Strukturen und Abläufen. Um den Job Auditor auszuüben, sollte man ein betriebswirtschaftliches Studium absolviert haben, vorrangig mit den Schwerpunkten Rechnungswesen, Revision oder Controlling. Zudem werden meist zwei bis drei Jahre Berufserfahrung im Bereich der Wirtschaftsprüfung und Auslandspraktika vorausgesetzt. Es werden Auditoren gesucht in den verschiedensten Unternehmen und Branchen. Stellenangebote Auditor bieten die Jobbörsen in der Schweiz und anderswo.

Jobs in Neuenburg (französisch Neuchâtel) werden in den verschiedensten Branchen und Firmen angeboten. Wer auf der Jobsuche in Neuenburg ist, findet häufig im Internet bei der Jobbörse JobScout24 offene Stellen. Bereits seit dem 18. Jahrhundert ist Neuenburg ein bedeutender Standort der Schweizer Uhrenindustrie und noch heute werden hier Zeitmesser für weltbekannte Uhrenmarken wie z. B. Bulgari hergestellt. Die Tradition der Präzision und Innovation wird heute vor allem in zahlreichen mittelständischen Neuenburger Firmen fortgesetzt, die in der Mikrotechnik und Präzisionsindustrie tätig sind. Sie produzieren Werkzeugmaschinen, Hochtechnologie, Elektronik und Medizinaltechnik. Die Ansiedlung vieler Firmen bewirkte nicht zuletzt das in Neuenburg befindliche, international anerkannte Institut CSEM (Centre suisse d’électronique et de microtechnique SA, Schweizerisches Zentrum für Elektronik und Mikrotechnik AG), das in Zusammenarbeit mit Wissenschaftlern aus aller Welt die Entwicklung von hoch technologischen Produkten fördert. Neben den kleinen und mittelständischen Firmen bieten daneben große internationale Unternehmen wie die Philip Morris AG oder Baxter, ein Spezialist für Biotechnologien, in Neuenburg häufig offene Stellen an. Auch der Tertiärsektor ist in Neuenburg vertreten. In der Stadt und der Region haben sich zahlreiche Banken, Finanz- und Treuhandgesellschaften niedergelassen. Wer eine Arbeit in Neuenburg sucht, sollte zuerst im Internet die Jobbörse JobScout24 aufsuchen. Hier finden sich jederzeit aktuelle Stellenanzeigen.

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Stellen zum Suchbegriff Auditor finden sich auch in folgenden Orten:

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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 are anchored in the internationally applicable Credo.


 


DePuy Synthes Companies of Johnson & Johnson is the largest, most comprehensive orthopedic and neurological business in the world. DePuy Synthes offer an unparalleled breadth and depth of technology, devices, services and programs in the areas of joint reconstruction, trauma, spine, sports medicine, neurological, cranio-maxillofacial, power tools and biomaterials. Our broad array of inspired, innovative and high-quality offerings, help advance the health and wellbeing of people around the world.


 


For our production site, we are looking for a highly committed: 


 


 

QC Team Leader

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 are anchored in the internationally applicable Credo.

 

DePuy Synthes Companies of Johnson & Johnson is the largest, most comprehensive orthopedic and neurological business in the world. DePuy Synthes offer an unparalleled breadth and depth of technology, devices, services and programs in the areas of joint reconstruction, trauma, spine, sports medicine, neurological, cranio-maxillofacial, power tools and biomaterials. Our broad array of inspired, innovative and high-quality offerings, help advance the health and wellbeing of people around the world.

 

For our production site, we are looking for a highly committed: 

 

 


Further responsibilities and duties are

  • Management of the Quality Control Team (several associates for: Receiving Inspection and Release) and ensures continuous supply of raw material to base business.
  • Manages and ensures KPIs are reviewed regularly and actions are taken as required
  • Responsible for conducting quality assurance inspections. Uses results, considerable judgment and initiative to improve production processes and standards.
  • Performs advanced tests and analyses to assure that products comply with established specifications.
  • Carries out complex calculations and documents test results.
  • Writes and/or reviews technical reports, develops charts, graphs, schematics and drawings to illustrate improvement processes.
  • Ensures tools and test equipment are properly calibrated and repaired according to standard operating procedures.
  • Applies nonstandard test techniques where standard procedures do not fulfill testing needs.
  • Makes recommendations on improving quality, efficiency, cost of company product(s), processes, and/or productivity techniques.
  • Ensures all documentation is recorded properly and follows standard operating procedures.
  • Determines methods and procedures on new assignments.
  • Applies in-depth knowledge and thorough practice.
  • Conduct investigation, bounding, product disposition, documentation, review and approval of Non-Conformances, CAPAs, Audit Observations and customer complaints.  Escalation of quality issues as appropriate.
  • Lead and maintain Material Review Board and maintain the quarantine area.
  • Analyze/review effectiveness of preventive and corrective actions.
  • Review root cause investigation according to an established process.
  • Conduct periodic warehouse audits to assess for production controls such as lot segregation.
  • Review results of area audits to ensure that corrective and preventive actions are adequate.
  • Provide guidance to project teams and business partners to ensure compliance with company policies and procedures as well as medical device regulations.
  • Partners with R&D and other cross functional partners to ensure the proper application of design controls, risk management and the investigation/correction of design failures/challenges and CTQ definition.
  • Supports the development of quality strategies related to the transfer of products, materials and components within J&J or externally.
  • Trains, coaches and develops associates to inspections and tests activities.
  • Supports new product introduction as part of design transfer.
  • Lead of quality projects: Lean projects, Inspection optimization, implementation of CMM equipment’s and reduce cost of inspection.
  • Supports and promotes the safety and industrial hygiene objectives of the plant.
  • CO document Implementation and Approval.
  • Product final release (restricted status vs non-restricted status).
  • Product in-coming inspection.
  • Internal/ External auditor.
  • Quarantine and restricted area management.
  • Product disposition in Non-Conformance, Block, accept or reject lots.
  • Authority to place product on hold or processes on hold.
  • Performs Annual Performance appraisals for the identified associates. Establish objectives and development plans for direct reports or applicable processes.
  • Interviewing, hiring, planning, assigning & directing work, mentoring, rewarding and disciplining employees, addressing complaints, resolving problems and issues.

 

Requirements

  • Engineering degree or equivalent.
  • Medical Device, ISO 9000, ISO 13485, 21CFR820 and GMP Knowledge.
  • Quality Control expert, excellent GD&T (Geometric dimensioning and tolerancing) skills.
  • Quality ans Lean Tools Knowledge.
  • Excellent Team management skills.
  • Good level in written and spoken French.
  • Proactive and able to take decisions.
  • Well organized and systematic approach to issues.
  • Able to work in a team with a strong leadership, Analytical skills, Sense of urgency.
  • Technical training and experience using Risk analysis (PFMEA), Statistics skills, Lean and Six Sigma Methodologies is required including Measurement System Analysis, SPC, DOEs, Gage R&R, etc.
  • Knowledge of statistical software packages is preferred with the ability to preview, graph and analyze data and be able to present data that facilitates/drives decision making.
  • CMM programs development a plus.
  • GD&T (Geometric dimensioning and tolerancing) and technical drawing knowledge and challenge the control plan definition.
  • Understanding of the NPI (New Product Introduction) process and Process Validation expertise is preferred.
  • A thorough understanding of GMP regulations and ISO standards and validation regulations is preferred.
  • Team player and excellent communication skills.
  • Leader as role model, Ensure Credo behaviors and expected behaviors are applied at the site.
  • Fosters teamwork and supports total associate involvement.

If you want to be a change agent in a challenging environment and shape the future quality organization, please send us your online application (CV, Motivation Letter, Working References etc.).

Kontaktperson

Website http://www.jnj.ch

Gesamtbewertung

1,7

Basierend auf 3 Bewertungen

3,0 Karriere / Weiterbildung
1,0 Gehalt / Sozialleistungen
Work-Life-Balance
4,0 Management

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