Chief Quality Assurance Specialist for Medical Devices

hace 1 mes


Málaga, Málaga, España D Healthcare A tiempo completo
About D Healthcare

We are an integral part of the globally renowned D.Med Healthcare Group, headquartered in Düsseldorf, Germany. With a rich history spanning over 80 years of combined experience in software engineering, medical expertise, and sales, we have rapidly grown into a dynamic company specializing in advanced software systems for the medical industry.

Our Mission

Our primary mission is to empower our clients to succeed by providing them with unparalleled cybersecurity solutions and fostering long-term partnerships built on trust and reliability. We specialize in providing cutting-edge cybersecurity solutions tailored specifically for the embedded systems in the medical industry, ensuring compliance with international standards.

Career Opportunities

We are seeking a Chief Quality Assurance Specialist for Medical Devices to join our team and lead quality testing in embedded medical devices, ensuring that our products meet the highest standards of safety and performance.

Job Description
  • Contribute to the whole life cycle of the software development process with a strong focus on testing and validation.
  • Design, plan, and execute hardware and software tests for embedded medical devices, ensuring compliance with industry-specific regulations and standards.
  • Develop and document test cases, test plans, and validation protocols to ensure system functionality and quality.
  • Coordinate and perform product verification and validation testing at different development phases (unit, integration, and system testing).
  • Collaborate with development, engineering, and product teams to identify issues, conduct root cause analysis, and propose improvements and corrections.
Requirements
  • Over 5 years of experience in embedded systems and platform integration testing.
  • Familiarity with test automation tools and frameworks.
  • Proven expertise in system and software validation.
  • Competence in C/C++ and Python.
  • Familiarity with regulatory requirements and industry standards for medical device software (e.g., IEC 62304, FDA guidelines) is highly desirable.
  • Well-founded knowledge in agile software approaches, preferably SCRUM, is desired.
Salary and Benefits

The estimated salary for this position is approximately €70,000 - €90,000 per year, depending on experience. In addition to a competitive salary, we offer a comprehensive benefits package, including health insurance, retirement plan, and paid time off.



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