Quality Manager Continual Improvement (m/w/d) - 80-100%
Belimed
Switzerland (Zug)
vor 2 Tg.

Quality Manager Continual Improvement (m / w / d) - 80-100% Belimed is a leading global supplier of innovative cleaning, disinfection and sterilization solutions for medicine, with subsidiaries in Europe, USA and China.

Under the brand name Belimed we develop, produce and distribute equipment for hospitals and clinics.

Our more than 1000 employees in 10 countries have been working tirelessly for over 50 years to provide our customers with absolute confidence in sterile processing solutions.

Would you like to join the team in Zug?

Your tasks The Quality Manager CIP is responsible for controlling of the continual improvement processes as well as for supervising the quality of CAPA documentation within the Belimed group.

Furthermore the QM CIP is also responsible for maintaining, improving and implementation of the integrated management system of the Belimed group and acts also as Business Analyst for QM / RA.

  • Controls the cases in the CAPA Management System regardingDocumentation qualityTime deadlinesEfficacy of Corrective and Preventive Actions
  • Supports the operation of the CAPA Management System and understands the meaning of Non-Conformance handling processes such as audit findings, non-conformance, complaints, investigations and reportable incidents
  • Performs trainings of users in CAPA processes
  • Acts as interface between users of the CAPA Management Tool (super user), determines further developments of the CAPA Management Tool
  • Supports the quality organisation in maintaining, improving and implementation of the integrated management system (IMS)
  • Prepares and manages the yearly audit planning and executes internal audits
  • Takes part during audits / inspections of Notified bodies or authorities
  • Supports regulatory affairs
  • Supports the Business Units and plants in quality and regulatory questions
  • Your profile

  • Bachelor or Master degree (Sc. Tech, Quality Management, Medical Engineering) with experience in the field of quality management in medical device context
  • German mother language, English Advanced C1
  • Quality management in the field of medical devices
  • Directives, regulations and standards for medical devices quality systems : MDD 93 / 42EU, MDR 2017 / 745, EN ISO 13485, EN ISO 14971, 21CFR Part 820 Quality System Regulation;
  • Part 803 Medical Device Reporting; Part 806 Medical Device Corrections and Removals; Part 821 Medical Device Tracking

  • MS Office (needed), SAP (welcome)
  • Our offer Use your background or interest in quality management to contribute to the success of our products. We offer you a key role in a dynamic and international company, committed to improving the safety of patient and staff worldwide.

    We are looking forward to your application (including CV, motivational letter and reference letters) via our online platform.

    Join our team and take your career further.

    In case of dossiers from employment agencies, the terms and conditions for the placement are negotiated individually in each case.

    General conditions are not accepted.

    Belimed AG processes personal data in accordance with the Belimed privacy statement available under : .

    6300 Zug

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