Manager Reprocessing/Wiederaufbereitung Medizinprodukte (m/w/d)

Aplitrak - Hamburg - 24-10-2019 zur Vakanz  

Als Personalberatung haben wir uns im Jahr 2007 auf die Medizintechnik-Branche spezialisiert. Mit einem Team von acht Beratern im Medical Device Bereich betreuen wir unsere Bewerberinnen und Bewerber innerhalb des kompletten Bewerbungsprozesses. Konkret bedeutet dies, dass wir Sie in allen Fragen rund um Ihren nächsten Karriereschritt beraten, Ihnen in der Zusammenstellung und Optimierung Ihrer Bewerbungsunterlagen helfen und Sie gezielt auf die Bewerbungsgespräche vorbereiten.

 
Zum nächstmöglichen Zeitpunkt suchen wir für den Standort Hamburg einen

Manager Reprocessing & Infection Control EMEA / Experten für die Wiederaufbereitung von Medizinprodukten (m/w/d)

 
The Manager Reprocessing & Infection Control EMEA owns a staff position within the organization. With its comprehensive know-how and knowledge on the reprocessing of medical devices the job holder supports other areas such as product marketing, QARA Global, Sales and Service, and the parent company. In addition, he/she manages the interface and cooperation with the manufacturing site on issues regarding cleanroom production and processing.

 

Key responsibilities / main tasks

  • Management of necessary post processing validations for Medical equipment and accessories (especially under European requirements)
  • Management of compatibility tests (including material compatibility testing) and evaluation / authorization of AER-devices and Medical devices and accessories
  • Preparation / review / approval of appropriate validation protocols and reports in cooperation with the respective Design Center, if required
  • Cooperation and advice on questions of processing and infection control (eg manual and mechanical processing, material compatibility) for EMEA Medical customers and distributors
  • Support of the QARA department / vigilance / product marketing in the areas of processing and infection control (eg hygiene report complaint assessment, specifications of new endoscope, product approval procedure)
  • Assistance in verificationof all informationandcomparisonwith national and international regulations. Review ofmanualsforreprocessing (ISO 15883-4, validationprotocol, ISO 17664). Promotingthehygienetopic via
  • Support in Processing & Infection Control external parties
  • Service support (customer advice, training events)
  • Support oftheoccupationalsafetyofficer in hygienetopics
  • Supports on issues regarding cleanroom manufacturing and cleanroom monitoring
 

Qualifications

  • Academic Study of relevant subjects
  • Several years of professional experience beneficial
  • Very good knowledge of standards and guidelines in the area of hygiene (national and international)
  • Preparation of medical devices
  • General product knowledge (endoscopes, Wassenburg)
  • Experience in employee and team leadership,
  • Mastery of common management tools
  • Mastering techniques of moderation, communication and presentation
  • MS Office (Word, Excel, Powerpoint)
  • Very good knowledge of English
 
Wenn wir Ihr Interesse wecken konnten, schicken Sie uns Ihre Bewerbungsunterlagen an johanna.vonwendt (a) progressive.de
 
Wir setzen uns gerne kurzfristig mit Ihnen in Verbindung, um die Position detailliert und vertraulich zu besprechen.
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