Need submission details for Senior Verification Engineer, Pleasanton, CA, Onsite

Dear Partner, Good Morning ,Greetings from Nukasani group Inc !, We have below urgent long term contract project immediately available forSenior Verification Engineer, Pleasanton, CA, Onsite need submissions you please review the below role, if you are available, could you please send me updated word resume, and below candidate submission format details, immediately. If you are not available, any referrals would be greatly appreciated. Interviews are in progress, urgent response is appreciated. Looking forward for your immediate response and working with you. Candidate Submission Format - needed from youFull Legal NamePersonal Cell No ( Not google phone number)Email IdSkype IdInterview AvailabilityAvailability to start, if selectedCurrent LocationOpen to RelocateWork AuthorizationTotal Relevant ExperienceEducation. / Year of graduationUniversity Name, LocationLast 4 digits of SSNCountry of BirthContractor Type : mm / dd Home Zip Code Assigned Job Details Job Title : Senior Full Stack Software EngineerLocation : Charlotte, NC, HybridRate : Best competitive rate Job Summary : Manual Protocol Tester to support software verification activities for web-based applications integrated with heart failure / medical devices. The ideal candidate will have hands-on experience in protocol-based testing, medical device software verification, and compliance with regulatory standards. Medical class II or class III is a must Strong communication and presentation skills is a must IEC medical standards is a must Key Responsibilities : Execute manual protocol-based testing for web applications supporting heart failure device workflows. Review and validate software requirements, design specifications, and protocol documents. Develop and maintain test protocols, test cases, and test reports in alignment with regulatory standards. Perform functional, integration, regression, and system-lent. Document and manage defects using tools like JIRA or equivalent. Ensure traceability between requirements, protocols, and test results. Collaborate with cross-functional teams including R&D, Quality Assurance, and Regulatory Affairs. Support verification and validation (V&V) activities and contribute to design history file (DHF) documentation. Ensure testing activities comply with FDA standards. Required Qualifications : Bachelor’s degree in engineering, Computer Science, Biomedical Engineering, or related field. Minimum 5 years of experience in manual protocol-based testing and within the medical device industry is plus. Strong understanding of web application testing and clinical workflows related to heart failure management. Experience with protocol writing, execution, and documentation in a regulated environment. Familiarity with regression analysis, risk management, traceability matrices, and compliance documentation. Excellent communication and analytical skills.