Change Control Specialist job opportunity at Abbott.

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DatePosted 3 Days Ago bot
Abbott Change Control Specialist
Experience: 6-years
Pattern: full-time
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degreeHigh School (S.S.C.E)
loacation Switzerland - Zurich, Switzerland
loacation Switzerland - ..........Switzerland

      JOB DESCRIPTION: 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 and   modify   all   product and process documentation   using   PLM   and ERP   software   packages.   Be a part of the   process engineering   team with extensive   interactions with the   R&D   and   Quality department s.   Ensure traceability and   compliance of the documents with the Quality templates and instructions   as well as   global   regulatory requirements.       Qualifications   Technical   degree s   in   Technical/scientific   fields. 3   to   6   years of experience   in   Engineering, Quality or Technical Writing   at a manufacturing environment.   Experience with medical device manufacturing   of electro-mechanical equipment.   Good written and oral   English   communication skills. German   speaking   an advantage.   Previous e xperienc e with   some   PLM   and   ERP   software   packages   i deally with   Windchill   and SAP.   Familiarity with   IT   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 the   centre   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.          The base pay for this position is N/A In specific locations, the pay range may vary from the range posted.       JOB FAMILY: Manufacturing       DIVISION: HF Heart Failure          LOCATION: Switzerland : Technoparkstrass 1 CH 8005       ADDITIONAL LOCATIONS:       WORK SHIFT: Standard       TRAVEL: No       MEDICAL SURVEILLANCE: Not Applicable       SIGNIFICANT WORK ACTIVITIES: Not Applicable                  

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