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Change Control Specialist

Change Control Specialist

Change Control Specialist

Change Control Specialist

Abbott GmbH

Medizintechnik

Zürich

  • Art der Beschäftigung: Vollzeit
  • 83.000 CHF – 102.500 CHF (von XING geschätzt)
  • Vor Ort
  • Aktiv auf der Suche

Change Control Specialist

Über diesen Job

Thoratec Switzerland GmbH is part of Abbott Laboratories, one of the world’s leading companies in medical devices and healthcare. We are the global market leader for implantable and extracorporeal blood pump systems based on magnetic bearings. Our lifesaving medical devices, which are developed and produced on-site in Zurich, are used for the short- and long-term treatment of patients suffering from severe heart disease.

Our Zurich site employs approximately 150 people, covering areas including R&D and manufacturing. Currently, we are expanding our innovative and high-caliber team in Zurich and an exciting opportunity exists for a motivated and talented software engineer.

Change Control Specialist - Medical Device

As part of the process engineering team you will support the team in creat ing , edit ing and manag ing the documentation regarding manufacturing processes, part specifications , inspection procedures and the design. You will help the manufacturing team to ensure that the product and project documents are properly managed and traced and approved by the management and all changes to the product or process are correctly reflected in all modified documentation. This position does not requires per se a strong technical background, but good understanding of MedTech/Pharma environment, good communication skills and a n independent problem-solving mindset.

Main Activities

  • Create, edit, manage andmodify all product and process documentation using PLM and ERP software packages.

  • Be a part of theprocess engineering team with extensive interactions with the R&D and Quality department s.

  • Ensure traceability andcompliance of the documents with the Quality templates and instructions as well as global regulatory requirements.

Qualifications

  • Technical degree s in Technical/scientific fields.

  • 3to 6 years of experience in Engineering, Quality or Technical Writing at a manufacturing environment.

  • Experience with medical device manufacturingof electro-mechanical equipment.

  • Good written and oralEnglish communication skills. German speaking an advantage.

  • Previous e xperienc e with some PLM and ERP software packages i deally with Windchill and SAP.

  • Familiarity withIT data services and regulated document authentications and safeguards.

What We Offer

  • A challenging position in a fast-growing crisis independent industry

  • To become part of a young, dynamic, highly educated, highly skilled, and motivated team

  • Flat hierarchies, open appreciative mentality, and efficient, constructive lines of communication

  • Multi-national environment, where we foster the development of our talents within the enterprise

  • Competitive compensations and benefits

  • A workplace in thecentre of Zurich with R&D and manufacturing under one roof

Looking forward to receiving your application documents including CV, motivation letter, and job certificates in PDF format.

Gehalts-Prognose

Unternehmens-Details

company logo

Abbott GmbH

Medizintechnik

10.001 oder mehr Mitarbeitende

Wiesbaden, Deutschland

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