Software Verification Lead

2 weeks ago

Pittsburgh, United States Rose International Full time

Date Posted: 10/29/2024

Hiring Organization: Rose International

Position Number: 473537

Job Title: Software Verification Lead

Job Location: Indianola, PA, USA, 15051

Work Model: Hybrid

Employment Type: Temporary

Estimated Duration (In months): 7

Min Hourly Rate($): 65.00

Max Hourly Rate($): 75.00

Must Have Skills/Attributes: Automation Testing, DevOps, Python, Software Testing

Job Description

***Only qualified Software Verification Lead candidates located near the Indianola, PA area to be considered due to the position requiring an onsite presence***


Education Requirement:

• Bachelor's degree in Computer Science or equivalent subjects


Required Skills for the Digital Solutions Software Verification Lead:

• Minimum of 8 years or more of relevant work experience in software testing, software engineering, requirement engineering and/or risk engineering in healthcare software development or other regulated software development

• Minimum of 5 years or more of Test Architect experience in Software Verification in healthcare software development or other regulated software development

• Minimum of 5 years of V&V engineering and design controls in healthcare software development or other regulated software development

• Minimum of 3 years of Test Automation experience in Software Verification and Leading QA teams

• Minimum of 2years experience in DevOps activities

• Technical writing ability – clear and concise writing easily understood by multiple audiences (testers, developers, auditors, peers, etc.)


Preferred Skills:

• Prior experience of working in Quality Systems Regulations with knowledge of documentation systems (i.e., Verification/Validation Protocols, SOPs) required of a business in the regulated industry

• Prior experience designing and developing medical device software in a regulated environment while adhering to FDA Design Controls and software process guidelines for medical devices including ISO 13485, IEC 62304, IEC 82304 and FDA Design Controls CFR 820.30

• Distinct conceptual and result-oriented thinking as well as customer orientation, high flexibility, and resilience

• Work experience in an international environment and fluent language skills (spoken and written) in English

• Knowledge of testing medical imaging algorithms and/or machine learning in the cloud

• Prior experience with scrum and test-driven development methods


The Software Verification Lead is responsible for software verification and validation of our class II and higher regulated AI/ML SaMD products. The Software Verification Lead is provides guidance and support for non-senior and external Quality Assurance Engineers as well as Leads and is responsible for process improvements in the software verification area as well as in the software requirement area. Software verification comprise but is not limited to engineering of software verification and validation, requirement engineering, development of test strategy, deploy and maintain CI/CD (DevOps) pipelines along with execution and reporting of test.


Responsibilities:

• Verification and Validation of software as a medical device including AI/ML based solution.

• Architect test strategy, development and execution of manual and/or automated software verification protocols, including

• Requirement analysis and review

• Architect test strategy

• Design and development of test scenarios

• Authoring and review of test cases and protocols

• Performing execution of test cases

• Analyzing results, tracking discrepancies, and writing reports

• Deploy and maintain CI/CD (DevOps) pipelines, including:

• Developing and maintaining Continuous Integration Deployment Testing infrastructure to accelerate product development cycle time

• Maintain test automation framework for medical device products

• Automating build creation and deployment, using Jenkins, AWS, and GitLab

• Scripting using Python, Perl, and other scripting languages

• Lead and manage verification and validation of complex AI software projects with cross functional teams distributed across multiple geographies under new product development (NPD) and/or Life Cycle Engineering (LCE) initiatives of ML/AI based Software as a medical device development, provide guidance and consulting to the team on technical and process issues, review deliverables of the team

• Fulfilling activities to comply with the project deliverables outlined in the Design and Development Plans and Design Control Procedures, as applicable.

• Compliance with standard operating procedures for medical device development, including compliance with ISO 13485, IEC 62304, IEC 82304 and FDA Design Controls CFR 820.30

• Individual contribution as well as managed activities involving verification planning, test execution and software integration.

• Critical analysis of technical situations to identify problems, and work with the cross-functional team in resolving the problems.

• Collaborating within cross-functional teams (technical lead, product manager, risk manager, software engineer, medical & clinical affairs and regulatory affairs) across multiple geographies to convey problems, opportunities, solutions, and results in software development activities

• Engaging in continuous improvement initiatives to establish Center of Excellence (CoE) in Software Assurance function


  • **Only those lawfully authorized to work in the designated country associated with the position will be considered.**


  • **Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client’s business needs and requirements.**


Benefits:

For information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website.

California Pay Equity:

For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here.

Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances.

If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise, please contact our HR Department.

Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E-Verify). (Posting required by OCGA 13/10-91.).

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