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工作内容
Nous sommes actuellement à la recherche active d’un test engineer pour l’un de nos clients actif dans le secteur pharmaceutique. Envie de nouveau challenge? N’hésitez plus : stessy.de.schutter@cx.ausy.be
#engineer#electronic#pharmaceutical
A degree in Science or Engineering; with a multidisciplinary background
- Minimum 5 years experience in Medical physics or engineering (Electronics, software, Biomedical engineering…)
- Experience in systems engineering disciplines is a must; preferably in a company designing complex, large-scale, critical systems (Test engineering, requirements engineering, quality…)
You have one or more of the following experiences:
Strong experience in Software quality assurance; including implementation of test strategies, automated testing design and usability engineering- Experience in designing Radiation therapy treatment control is a strong plus
- Experience in using, configuring or designing Oncology Information Systems or Treatment Planning Systems is a strong plus
- Interaction with internal and external third parties, including Product Management representative, customer representative, third-party representatives, regulatory authorities
- Proficient use of a Requirements and test management tool (DOORS; Polarion, Helix, …) is a strong asset
- Excellent oral and written communication skills in English;
And you are:
- A team player able to communicate / facilitate / focus on promoting solutions, even in exposed situation (towards management or regulatory authorities)
- A quick learner, willing to build a solid competence in his field and take, over time, broader challenges
- Capable of thinking cross-functionally
- You have a strong sense of structure and rigorous documentation skills
- Quality focused, working for the highest value for your stakeholders, with integrity
- You are ready to travel up to 10 % of your time
A worldwide company in the pharmaceutical field !
As a Requirements & Verification expert in the Systems Engineering department, Requirements & verification group, you will take part in the design and development of world leading solution for image guided Proton Therapy and other medical diagnostic and sterilization applications using ionizing radiations.
You’ll have the opportunity of participating in cross-functional project teams ensuring integration of Proteus 235 with Third-party devices and software (OIS, TPS, …) and the treatment control system of Proteus 235.
You will share responsibility of the management of system requirements and system testing for an effective product with the highest customer value. In this role, you will ensure that your work complies with the highly regulated environment of medical applications using ionizing radiations:
- You take part in requirements engineering activities for new projects and product changes. You negotiate with project stakeholders, allocate and flowdown system requirements of the proton therapy products, trace them and document them in a complete and consistent way in DOORS.
- You ensure design verification engineering practices by defining test plans, test methods, analyses, design reviews and performing tests
- You take part in the improvements of system engineering methods and tools by collecting, suggesting and implementing changes in agreement with the experts
- You promote and support harmonized practices compliant with regulations and company procedures
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最后期限: 10-01-2026
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