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Quality Engineer - Medical Manufacturing

Swisstech Recruitment

Posted on Jan 4, 2021 by Swisstech Recruitment

Zug, Switzerland
Health Care
Immediate Start
Annual Salary
Contract/Project


Tasks and areas of responsibility:

  • Monitoring and securing the quality of the assigned products, as well as carrying out the
    technical approval of the assigned products
  • Knowledgeable about the manufacturing process and specialist in the testing processes at our external partners
  • Quality-side project responsibility
  • Responsibility for qualification of internal and external test methods and test equipment
  • Implementation of the test data collection, processing and interpretation
  • Maintaining the test specification documents and instructions including training
  • Act as an expert in complaint management as well as problem solving and
    escalations
  • Test equipment owner of internal and external test systems

Side tasks:

  • Management or participation in special tasks/projects (creation, improvement of processes, engineering studies, etc. and processing of change tasks/CAPA tasks)
  • Assistance with budget planning and investments
  • Participation in or management of organizational development projects
  • Participation in the introduction of new employees
  • Continuous improvement of processes

Requirements

  • University or technical college degree in mechanical engineering/medical technology/scientific/technical direction
  • Basic technical training (EFZ) in the field of plastics technology, toolmaking, polymechanics or similar. with practical experience in quality assurance or in the diagnostic/molecular biological laboratory is an advantage
  • First professional experience in the area of 'six Sigma methodology, quality assurance, quality technology, test planning
  • Experience in measuring equipment and process qualification (eg cpk; MSA)
  • Several years of experience in serial production companies and in assessing/understanding semi-automated and fully automated production lines
  • Practical experience in the regulated GxP environment, ideally in medical technology or IVO (ISO e13485, GMP, FDA 21 CFR 820)
  • Proactive approach when recognizing deviations, grievances and sources of error
  • Enthusiasm for the close cooperation with plastic products and their manufacturing process at the supplier (also in the clean room)

For all positions based in Switzerland, SWISSTECH Recruitment works with their SECO licensed Swiss partner Accurity GmbH to ensure that candidate applications are handled in accordance with Swiss law. Please submit applications and direct any enquires directly to SWISSTECH Recruitment.




Reference: 1050952033

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