Our Client:

A medtech client in Selzach

Job Description:

• As complaint handling specialist for medical devices you are responsible for the structured investigation of claimed products.
• You will do device inspection and root cause analyses on these claimed products and based on your findings initiate corrective actions if necessary.
• Moreover you analyze engineering data, test certificates, risk evaluations, etc. and compile trendings. Your results are then documented in English in the international Stryker database.

The ideal candidate:

• You successfully completed your studies in a technical field (ideally mechanical engineering, quality management or medical technology) or alternatively you have completed your technical apprenticeship above-average and have already gained some work experience in a regulated environment.
• Ideally, you already have first experiences in complaint handling of medical devices (post market vigilance) and have had experience with the implementation of corrective actions (CAPA).
• You have a distinctive passion for technical matters, are an analytical thinker and like to work independently but also in interdisciplinary teams.
• Very good written and spoken English complete your profile. German and/or French is a plus.

Application process:

• CV to: m.burgstaller@sciproglobal.de
• Phone call including a presentation of the company
• I take over the whole application process (from interviews to contract negotiations)
• Discuss also other suiting options tailored towards your profile

My Contact:

• E-Mail: m.burgstaller@sciproglobal.de
• Tel: +41 43 508 92 17
• Xing: https://www.xing.com/profile/Michael_Burgstaller19/cv