An AI-enabled Vendor Management System designed to manage contingent workforce supply chain for medium and large organizations.VMS Vendor Management System, is a cloud-based software platform that solves a common problem for many global enterprises - how to find, engage, and manage its external workforce - both contract or contingent labor and services providers.

Plays a lead role in QA Efforts on multiple and possibly simultaneous projects.
Work on projects of moderate to high complexity that required in-depth knowledge across multiple technical areas and business segments.
Creating and maintaining various quality matrices is essential to understand the project\'s progress.
Liaise with PMs and BAs to understand the features and technical implementation.
Understand testing requirements, design and review test plans and strategies accordingly.
Analyze and report defects, track defect status and communication to the relevant stakeholders.
Writing and execution of test cases, analyzing results, and managing defects and issues using JIRA.
Carrying out detailed research and completing documentation and risk assessments.
Perform functional, regression and performance testing for web services.
Train and guide the resources by keeping up to date with the latest product features and end to end flow.

Develop blueprints, engineering plan, and graphics for products
Manage engineering records and designs
Develop test prototypes
Carrying out a detailed research and completing documentation and risk assessments
Overseeing implementation and conducting internal inspections and communication with others
Carrying out reviews of processes and adapting plans based on feedback
Producing training materials and sharing best practice throughout a business
Successfully developed and implemented the standards for SPE3000 and IEC60601-1
Successfully developed and implemented the standards for ISO9001, ISO13485, ISO14971
Successfully developed and implemented the standards for Medical Devices Establishment License (MDEL)
Performed the risk analysis for medical devices and developed standards to counter the risks
Developed documentation for medical devices for approval from FDA-CFR
Supervising technical staff for the standards implementations (ISO 13485, CFR, and MDEL)

Specifying quality requirements of raw materials with suppliers
Determining & negotiating in-house quality procedures, standards, and specifications
Investigating and setting standards for quality and health and safety
Working with operating staff to establish procedures, standards, systems, and procedures
Revising procedures, reports, etc. periodically to identify hidden risks or non-conformity issues
Writing management and technical reports
Directing objectives to maximize profitability
Recording, analyzing, and distributing statistical information (QC Tools)
Supervising technical staff for the standards implementations (ISO 9001 & ISO 13485)
Continuous improvement in the designs of products
Assessed the usability, environmental impact, and safety of a design
Computer-aided design (CAD) and computer-assisted engineering (CAE) software to create prototypes
Collect and Analyze data from tests on prototypes

Research and draft blueprints, engineering plans, and graphics
Develop test prototypes
Use design software to develop models and drawings of new products
Maintain existing engineering records and designs.
Assess all engineering prototypes to determine issues or risks
Supervise the manufacturing process of all designs
Supervision in material selection
Team management & resource utilization
Collect and Analyze data from tests on prototypes