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3 Process Application Consultant Stellen in Basel gefunden

Process Application Consultant Jobs in Basel

Als eine der schweizer Metropolen bietet Basel mehr als 650.000 Arbeitsplätze. Ganz sicher finden auch Sie passende Jobs in Basel. Offene Stellen findet man z.B. in der Chemie- und Pharmabranche, da solche Weltkonzerne wie Clariant, Novartis oder Roche in Basel ansässig sind. Basel ist einer der wichtigsten Standorte der chemischen und pharmazeutischen Industrie im Land und bietet zahlreichen Fachkräften entsprechende Arbeit. Ebenso offeriert Basel als einer der größten Bankenplätz in der Schweiz vielfältige Stellenangebote bei Banken und Versicherungen, nicht nur bei internationalen Großbanken oder privaten Bankhäusern, sondern auch bei der Schweizer Nationalbank oder der Bank für Internationalen Zahlungsausgleich. Aufgrund der günstigen geographischen Lage spielt die Transport- und Logistikindustrie eine wesentliche Rolle für offene Stellen in Basel. Neben dem Logistikdienstleister Panalpina und der SBB Cargo, der für den Güterverkehr zuständigen Tochtergesellschaft der Schweizerischen Bundesbahn, hat auch die schweizerische Fluggesellschaft Swiss ihren Sitz in Basel. Traditionell in Basel beheimatet sind zahlreiche Verlagen und Druckereien, bei denen die Jobsuche sich auf jeden Fall lohnt. Als Standort der Medienindustrie kann der Jobsuchende mit etwas Glück bei Zeitungen, Radio- oder Fernsehsendern Stellen in Basel finden. Eine Suche auf JobScout24 nach aktuellen Stellenangeboten für Basel lohnt sich daher. Schauen Sie sich regelmäßig die Stellenanzeigen für Basel an.

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Stellen zum Suchbegriff Process Application Consultant finden sich auch unter den folgenden Berufen:

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Quality Engineer / Validation Consultant

Quality Engineer / Validation Consultant
Our client is the largest, most comprehensive orthopedic and neurological business in the world. Their broad array of inspired, innovative and high-quality offerings helps advance the health and wellbeing of people around the world. On their behalf, we are looking for a
 
Quality Engineer / Validation Consultant
 
In this role, you will support manufacturing operations in the areas of process development, tool design, machine programming & layout, machinery & equipment, continuous improvement and other duties associated with engineering support of production. You will ensure, that all manufactured products meet the new EU Medical Device Regulations (EU MDR).
 
 
Your main tasks:
  • Support process validation strategy and write and executs engineering studies and process validation protocols and summary reports (Installation Qualification, Operation Qualification, Performance Qualification, Computer Software Validation and Test Method Validation)
  • Develop and implement control plans consistent with product classification, potential defect types, defect frequency, severity, patient risk, process capability, process controls
  • Develop and implement appropriate process monitoring and control methods consistent with the level of process/product risk
  • Assess and interpret common versus special cause variation in manufacturing processing and determine adequacy of current process limits
  • Ensure the development of a comprehensive risk management plan for the product and process
  • Document, justify, review or analyze whether a proposed change to a process will not enhance the risk level in some way beyond capability of current controls or whether change will result in potential noncompliance to a required standard such as the QSRs
  • Assess the need for risk mitigation techniques given product classification, potential defect types, defect frequency, severity, patient risk, process capability, process controls, etc. Determine effectiveness of these techniques on previously implemented improvements
  • Assists in the development of manufacturing and inspection procedures.
  • Support the Manufacturing Organization in creation, review and release of MPI & Risk Management Activities
  • Responsible to originate/oversee/assist in the creation & release of change orders (COs) through Agile PLM software.
  • Conduct investigation, bounding, documentation, review and approval of non-conformances, CAPAs and customer complaints. Escalation of quality issues as appropriate.
  • Support Base Business and Production Improvement Initiatives
 
 
Your background
You enjoy working independently in a highly agile environment. You are able to communicate with various stakeholders with confidence, transparency, patience and tenacity. Furthermore, you are well organized and are able to multitask.
Following skills complement your profile:
 
  • BSc in Manufacturing Engineering, Mechanical Engineering, Industrial Engineering, or a related degree
  • Several years of experience in quality engineering in the medical device industry is a must (preferably with packaging, Laser, and CNC processes and equipment)
  • Experience with ISO 9000, ISO 13485 and GMP is a must
  • Experience in Design and Process validation and knowledge of Quality Tools
  • Six Sigma or Lean Sigma certification or 4 years of experience preferred
  • Knowledge and skills in PLM system, Agile PLM, SAP, Windchill, Adaptive is a plus
 
Assignment start: asap
Planned assignment duration: until the end of 2019
Workload: 100% (40h/week)
Workplace: Oberdorf (BL)
 
 
If you have the required experience and if you would like to apply for this interesting position, please send your complete application documents (CV, testimonials, diplomas) to nicole.blum(at)kellyservices.ch or apply online.
 
We are looking forward to getting to know you!

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