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You are responsible for
Review and Approval of designated project documentation in product creation projects.
Advise upper management with respect to release for delivery of products
Support and represent Q&R discipline in Design Reviews, Hazard Analysis brainstorms, Health Risk Assessments
Execution of audits in all business processes and report the findings to upper management
Support and advise the organization in corrective and preventive actions
Translates regulations and standards and bring them to consolidation in the organization and the Quality Management System
Responsible for performing timely, detailed SW Quality engineering tasks like: assessing software designs and reviewing test and other performance data, analyses market feedback, completing or assisting with in root cause analysis and SW Quality problem solving.
You are a part of
a senior resourceyou will be part of a team that works for different projects.
To succeed in this role, you’ll need a customer-first attitude and the following
Minimal of 8 - 10 years of relevant work experience
Bachelor or Master degree in relevant knowledge domain, e.g.: Computer Science , electronics, Electrical or information technology
Knowledge of relevant external standards for Quality Management Systems for medical devices (ISO 13485,IEC 62304)
Knowledge of product creation and (software) development methods & tools
Good communicator, Analytical, Problem solver
English both written and spoken.
In return, we offer you
Hybrid work flexibility means people can meet the changing demands of work and home in the most balanced, productive, and healthy way. Hybrid work flexibility means people can meet the changing demands of work and home in the most balanced, productive, and healthy way.
Our hybrid working model is defined in 3 ways:
We want to be at our best: The way we work and our workspaces are designed to support our well-being, offer career advancement opportunities, and enable us to be at our best.
Make a difference. The work of your life begins here
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