In this role, you will have the opportunity to:
Assessment of product requirements
Definition of test strategy, test methods, acceptance criteria, needed materials, applicable sampling plan etc.
Definition and development of test fixtures / test benches, special test environment and ensure they are adequate for the test purpose
Preparation of test protocols / test reports and reporting of identified issues
Execution of test cases / test protocols on system
Investigation of identified issues (root cause analysis, reproducibility steps etc.)
Collaboration with other functions (development, system engineering, QA) to define the appropriate approach for the above mentioned activities
Documentation on relevant tools
Supporting definition of the project test strategy, project plan and metrics
Supporting definition of process improvement, tools and laboratory management
Definition and improvement of test techniques
Support the Manager for team activities and mentoring other team members
Facilitate discussion within the team and with other departments
Troubleshooting of SW and HW problems
The essential requirements of the job include:
Experience with clinical labs and working in a regulated environment
Laboratory routine activities (e.g. operation, calibration and maintenance of instruments).
Bachelor’s or Master´s degree in a related field with minimum 2 years of relevant experience in manual testing/system verification.
Understanding of software development processes for a regulated environment (FDA/ISO13485) and experience in medical device verification is a plus.
Experience in Agile and Scrum principles and ISTQB foundation certification or equivalent.
Ability to work independently while staying aligned with the functional team
Effective written and spoken communication skills in English
Ability to work with multi-functional and remote teams
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