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

Overview

On Site
$40 - $50
Contract - Independent
Contract - W2
Contract - 12 Month(s)

Skills

Testing/QA
verification/validation
Manual Testing
Healthcare testing
Protocal based testing
ICE/FDA

Job Details

Dear Partner,

Good Morning ,
Greetings from Nukasani group Inc !, We have below urgent long term contract project immediately available for Senior 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 you
Full Legal Name
Personal Cell No ( Not google phone number)
Email Id
Skype Id
Interview Availability
Availability to start, if selected
Current Location
Open to Relocate
Work Authorization
Total Relevant Experience
Education./ Year of graduation
University Name, Location
Last 4 digits of SSN
Country of Birth
Contractor Type

DOB: (dd/mm) mm/dd

Home Zip Code

Assigned Job Details

Job Title : Senior Full Stack Software Engineer
Location: Charlotte, NC, Hybrid
Rate : 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.

Thanks and Regards

Nancy
Talent Acquisition | Nukasani Group Inc
Tel:
Email:
;br />540 W Galena Blvd, Suite 200, Aurora IL 60506.

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