Technical Lead in Medical Device Testing
il y a 7 jours
Nipro Corporation Japan is a leading global healthcare company with over 33 years of experience. Our European headquarters in Mechelen serves as the base for Nipro Medical Europe, Nipro PharmaPackaging International, and the Institute for Medical Practice (iMEP) Belgium. As a fast-paced international business, we are committed to innovation and growth.
Job Description:
We are seeking a highly skilled R&D System Verification Engineer to join our team at Nipro Europe Group Companies (NEGC). The successful candidate will play a leading role in planning and executing verification tests during the development of new and existing dialysis equipment. This will involve developing test plans & procedures based on product and user requirement specifications and performing tests accordingly. You will be an integral part of our product ideation process, ensuring the quality of new and updated products from development to final product launch.
Key Responsibilities:
* Develop test setups using test and data acquisition equipment for measuring system performance
* Design test cases to include test methodology, test setups, materials, procedures, requirements and acceptance criteria
* Perform all tasks in accordance with ISO quality and JSOX requirements
* Engage with different product stakeholders to understand customer needs and design specifications, and translate these into test specifications
* Collaborate with cross-functional teams to ensure smooth product development and testing processes
Requirements:
* Bachelor or Masters degree in Biomedical, Electrical, Mechatronics, Control Systems or Mechanical Engineering
* A genuine interest in testing hardware, software and medical device systems
* Experience with designing or specifying test benches, data acquisition, measurement test setups and instrumentation
* Proficiency in at least one engineering programming language (e.g. MATLAB, Simulink, LabVIEW, Python, C)
* Strong attention to detail in specifying and documenting tests, following good documentation practice
* Familiarity with HIL / SIL automated test environments is a plus
* Experience working with medical device system verification and/or development is a plus
What We Offer:
* The opportunity to develop and grow in a fast-paced international business setting
* Collaboration with a talented team of professionals from around the globe
* Flexible work environment with opportunities for professional development and advancement
About You:
* Fluency in English (additional languages are a plus)
* Ability to occasionally travel within Europe to support testing activities at external partners and notified bodies
* Excellent communication and interpersonal skills
* Strong problem-solving skills and ability to adapt to changing priorities
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