Systems Test Engineers

Job Description

Role Overview:As a Systems Test Engineer, your main responsibilities will include testing and debugging critical sub-assemblies, conducting early dry run testing of system verification test procedures, and performing V&V activities for FDA and EUMDR remediation projects. You will be tasked with enabling and/or performing functional testing through the development of robust and reusable tests, working with design teams to isolate design errata, and supporting external teams to verify system performance. Additionally, you will be involved in supporting the test estimation and planning activities, ensuring that all verification activities are conducted in accordance with Quality System requirements, and following improvements in the profession of test engineering.Key Responsibilities:- Testing and debug of critical sub-assemblies- Conducting early dry run testing of system verification test procedures- Performing V&V activities for FDA and EUMDR remediation projects- Enabling and/or performing functional testing through the development of robust and reusable tests- Working with design teams to isolate design errata, perform failure analysis, and verify design fixes- Supporting and working collaboratively with external teams to verify system performance- Supporting the test estimation and planning activities- Ensuring that all verification activities are conducted in accordance with Quality System requirements- Following improvements in the profession of test engineeringQualifications Required:- Bachelors or Masters degree in Mechanical / Electronics / Electrical / Biomedical Engineering with a broad technical understanding and interest- Minimum 6 to 9 years of experience on system verification and validation of medical devices- Experience on V&V of ventilator will be preferred- Hands-on experience of test method validation- Hands-on experience of remediation projects for FDA or EUMDR- Understanding and compliance with Philips QMS- Technical documentation authoring and editing skills- Familiarity with quality procedures and documentation- Proficiency with MS Office, MS Excel, or equivalent- Good communication of both written and spoken EnglishAbout the Company:Philips is a health technology company dedicated to providing quality healthcare to all individuals worldwide. The company believes in the importance of every human life and aims to ensure access to quality healthcare for everyone. By joining Philips, you will have the opportunity to do meaningful work that impacts the lives of others positively. Role Overview:As a Systems Test Engineer, your main responsibilities will include testing and debugging critical sub-assemblies, conducting early dry run testing of system verification test procedures, and performing V&V activities for FDA and EUMDR remediation projects. You will be tasked with enabling and/or performing functional testing through the development of robust and reusable tests, working with design teams to isolate design errata, and supporting external teams to verify system performance. Additionally, you will be involved in supporting the test estimation and planning activities, ensuring that all verification activities are conducted in accordance with Quality System requirements, and following improvements in the profession of test engineering.Key Responsibilities:- Testing and debug of critical sub-assemblies- Conducting early dry run testing of system verification test procedures- Performing V&V activities for FDA and EUMDR remediation projects- Enabling and/or performing functional testing through the development of robust and reusable tests- Working with design teams to isolate design errata, perform failure analysis, and verify design fixes- Supporting and working collaboratively with external teams to verify system performance- Supporting the test estimation and planning activities- Ensuring that all verification activities are conducted in accordance with Quality System requirements- Following improvements in the profession of test engineeringQualifications Required:- Bachelors or Masters degree in Mechanical / Electronics / Electrical / Biomedical Engineering with a broad technical understanding and interest- Minimum 6 to 9 years of experience on system verification and validation of medical devices- Experience on V&V of ventilator will be preferred- Hands-on experience of test method validation- Hands-on experience of remediation projects for FDA or EUMDR- Understanding and compliance with Philips QMS- Technical documentation authoring and editing skills- Familiarity with quality procedures and documentation- Proficiency with MS Office, MS Excel, or equivalent- Good communication of both written and spoken EnglishAbout the Company:Philips is a health technology company dedicated to providing quality healthcare to all individuals worldwide. The company believes in the importance of every human life and aims to ensure access to qual

Keyskills :
System VerificationValidationMedical DevicesQuality SystemTechnical DocumentationMS OfficeMS ExcelQuality ProceduresVentilatorTest Method Validation