Medical Device Risk & Project Management

gloor & lang Pharma and Biotech Recruiting

Vue: 138

Jour de mise à jour: 04-04-2024

Localisation: Lucerne Luzern LU

Catégorie: Direction

Industrie: Staffing Recruiting

Niveau: Entry level

Type d’emploi: Full-time

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le contenu du travail

Innovative products for patients: Sensors - Applications - Devices

Ready to work with a manufacturer of application-oriented medical devices at the interface: development - market feedback - user risks?

Become a proactive and independent member of the team at our customer in the Bern region. Innovative mechanical products in connection with the latest electronics and software are translated into viable applications with cloud solutions for the use, the patient. At this point you are the liaison point between incidents that influence the ongoing product improvement and the corresponding technical documents.

Your tasks:
  • Analysis of market feedback: Complaints, CAPA, non conformity reports
  • Elaboration of product requirements according to feature analysis and user analysis
  • Determination of risk factors and strategic risk management
  • Identification of risk minimization measures in various project and product management teams

International standards such as ISO 13’485 or other regulated environments such as GMP do play a significant role in the documentation and application processes.

Your profile:
  • Training in technology (microtechnology, electronics, software, control technology) or natural sciences
  • Knowledge of process analysis, feature analysis, risk analysis
  • Experience of working in a regulated environment
  • Experience with risk analysis and risk project management ISO 14’971
  • Good knowledge of English, some German is an asset

You are a creative thinker, able to analyse data, processes and product use and contribute with ideas and viable suggestions. Interested? We are looking forward to get in touch with you.

Online application
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Date limite: 19-05-2024

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