Role Description We are looking for an experienced AI Platform Testing Engineer to join our team remotely and play a key role in ensuring the quality, performance, and reliability of our AI-powered platform before its official launch. The ideal candidate will have a strong background in software testing, an understanding of AI applications, and working knowledge of programming languages to effectively test, validate, and troubleshoot platform functionality. - Design, execute, and maintain test plans, test cases, and testing scenarios. - Perform functional, integration, regression, usability, and end-to-end testing. - Test AI features, prompts, workflows, and generated responses for accuracy, consistency, and reliability. - Identify, document, prioritize, and track defects through to resolution. - Validate bug fixes and perform regression testing before releases. - Test APIs, integrations, and system performance. - Ensure compatibility across browsers, operating systems, and devices. - Collaborate with developers, product managers, and AI engineers to improve platform quality. - Prepare detailed testing reports and provide launch readiness recommendations. - Suggest improvements to enhance platform stability and user experience. Qualifications - Experience with automation testing tools such as Selenium, Playwright, or Cypress. - Familiarity with CI/CD pipelines and Git. - Knowledge of SQL and database testing. - Understanding of Large Language Models (LLMs), prompt engineering, and AI model evaluation. - Experience working in Agile/Scrum development environments. Requirements - 3+ years of experience in Software QA, AI application testing, or platform testing. - Strong understanding of software testing methodologies and quality assurance best practices. - Experience testing web-based applications and AI-powered platforms. - Good understanding of programming languages such as Python, JavaScript, Java, C#, or similar. - Experience with API testing tools (e.g., Postman) and bug tracking tools (e.g., Jira). - Ability to understand application logic, troubleshoot issues, and communicate effectively with development teams. - Strong analytical, problem-solving, and documentation skills. - Excellent written and verbal communication skills. - Ability to work independently in a remote environment and manage priorities effectively. Company Description

Role Description Our client is an innovative manufacturer of medical devices in the United States which produces devices and software applications. At this project, you will have a great opportunity to be involved in the full development life cycle of medical software which is intended to help individuals by processing certain information taken from medical devices to identify health trends and track daily activities. Qualifications - At least 2-5 years of IT industry experience (Software Quality Assurance Engineer/Analyst/process engineer or similar position from Quality Assurance or Process Management sphere) or as a quality/certification/process/metrology specialist in other domains is a must; - Strong knowledge, deep understanding, and practical application (implementation, support) of international quality management system standards and regulations (e.g. ISO 9001:2015, ISO 13485); - Experience in auditing/assessment of Quality Management System based on international quality management system standards (e.g. ISO 9001:2015, ISO 13485, FDA Quality System Regulation (21 CFR Part 820)); - Experience in preparation/review of product-specific lifecycle documentation intended to confirm quality of the product; - Good understanding of Risk Management principles and techniques (Failure Mode and Effect Analysis (FMEA), FTA and other); - Good understanding of medical device SQA principles and related regulations: ISO 13485, IEC 62304, ISO 14971, FDA QSR Part 820, EU MDR; - Good understanding of software V&V methodologies and software development life cycle; - Good understanding of software testing principles; - Ability to work with big amounts of information, produce and organize content in a logical flow; - Strong documentation management skills, ability to review, analyze and interpret complex and complicated documents; - Good analytical skills; - Attention to detail and being a kind of perfectionist; - Ability to cope with quite routine work; - Team player; - English: Upper Intermediate or higher; ability to communicate with native speakers is a must; Requirements - Leading review and approve of project documentation (such as development plans and reports, verification test plans and reports etc.), providing feedback and support team in order to ensure timely preparation and readiness of project deliverables; - Review and approve of CSV documentation; - Assessing project activities and deliverables against established procedures, standards and regulations as per established QMS; - Advising R&D team regarding implementation or adjustment of established processes; - Work closely with engineering, product, and support teams to ensure the quality and accuracy of project deliverables; - Communicating with a customer on quality assurance, process management, documentation preparation topics; - You will collaborate with R&D and product management teams to ensure robust quality processes and regulatory compliance; - This role is critical for ensuring patient safety, product effectiveness, and successful regulatory submissions. Benefits - Empowering Projects: With 500+ clients spanning diverse industries and domains, we provide an exciting opportunity to contribute to groundbreaking projects that leverage cutting-edge technologies. As a team, we engineer digital products that positively impact people's lives. - Empowering Growth: We foster a culture of continuous learning and professional development. Our dedication is to provide timely and comprehensive assistance for every consultant through our dedicated Learning & Development team, ensuring their continuous growth and success. - DE&I Matters: At GlobalLogic, we deeply value and embrace diversity. We are dedicated to providing equal opportunities for all individuals, fostering an inclusive and empowering work environment. - Career Development: Our corporate culture places a strong emphasis on career development, offering abundant opportunities for growth. Regular interactions with our teams ensure their engagement, motivation, and recognition. We empower our team members to pursue their career goals with confidence and enthusiasm. - Comprehensive Benefits: In addition to equitable compensation, we provide a comprehensive benefits package that prioritizes the overall well-being of our consultants. We genuinely care about their health and strive to create a positive work environment. - Flexible Opportunities: At GlobalLogic, we prioritize work-life balance by offering flexible opportunities tailored to your lifestyle. Explore relocation and rotation options for diverse cultural and professional experiences in different countries with our company.

Role Description The CJIS Application Tester will be responsible for system testing, User Acceptance Testing (UAT), and validation of system requirements for the Connecticut Information Sharing System and other CJIS-managed applications. This role requires a strong understanding of enterprise-level system integration, API testing, automation framework development, and data validation. The tester will work closely with developers, project managers, and stakeholders to ensure system reliability, performance, and compliance with CJIS standards. Qualifications - Bachelor's degree in Computer Technology, Computer Science, or related field. - 5-7 years of experience in software testing or QA engineering within IT projects. - Experience testing large integrated enterprise systems. - Strong knowledge of automation testing frameworks. - Proficiency in Java or C# programming. - Experience with data-driven automation testing. - Knowledge of Extent Reports or similar automation reporting tools. - Experience with GitHub for version control. - Experience with SoapUI, Postman, and defect management tools. - Experience with IBM Rational Jazz Suite (preferred). - Experience with NIEM XML or complex XML standards. - Knowledge of Service-Oriented Architecture (SOA). - Ability to write complex SQL queries using Microsoft SQL Server. - Strong experience with API and web service testing. - Strong analytical and problem-solving abilities. - Excellent documentation and communication skills. - Ability to work effectively in cross-functional teams. - Proficiency in Microsoft Excel. Requirements - Strong understanding of enterprise-level system integration. - Experience with automation framework development. - Ability to ensure system reliability, performance, and compliance with CJIS standards. Benefits - Competitive salary. - Health and wellness programs. - Opportunities for professional development.

Role Description Join Us in Shaping the Future of Animal Health. Our Animal Health Division is investing $895 million in expanding our manufacturing and research & development facilities in De Soto, Kansas — the state’s largest economic development project to date. As a Sr. Specialist, Quality Control you will be part of a world-class team at our Center of Excellence in the Animal Health Corridor, contributing directly to the production of veterinary products that improve animal health and welfare globally. This role combines project leadership/coordination and quality oversight to ensure successful QC laboratory method transfers. The Quality Control Sr. Specialist will ensure laboratory processes and systems are in place to meet Quality Control testing activities associated with the method transfers. The successful candidate will collaborate with cross‑functional teams (Analytical Tech Support, Manufacturing, Validation, Quality Control) to identify gaps and risks, implement appropriate controls, and drive continuous improvement to support the project. Key Responsibilities - Serve as the Project lead for the QC laboratory transfers. - Serve as the liaison to the project sponsors, keeping them informed of the status of all project activities and resources. - Represent the team at project/tier meetings. - Evaluate site-to-site process/methods. - Resolve any Project Issues in an effective manner. - Ensure teams are formed to support the project, and monitor timelines to ensure that each phase is completed on schedule, preventing delays. - Coordinate site level activities related to the method transfers. - Ensure that deliverables meet quality standards before moving to the next phase. - Review/approve required test method information (spec sheets, tests, biomaterials/reagents, release criteria). - Review/approve protocols and reports associated with the project. - Support completion of Transfer Complexity assessment. - Author the Quality Risk Management Plan, and support gap assessments. - Coordinate Change Control plans and review/approve related Change Records. - Ensure readiness for sample management (sampling plans - transport and handling). - Support Regulatory Affairs with Outline of Production/Special Outline updates. Qualifications - Bachelor’s degree in Biology, Microbiology, Chemistry, Animal Science, Biotechnology, or equivalent experience. - 10+ years of progressive experience/roles within quality control in USDA-regulated animal product facilities. - Experience with USDA regulations and inspection processes in manufacturing environments. - Relevant practical experience with QC laboratory environments, method transfer, or related quality roles in biologics, vaccines, or similar industries. - Experience with qualification of facilities, equipment, instruments, and/or utilities. - Knowledge of Good Manufacturing Practices (GMP), quality systems, and regulatory expectations. - Strong attention to detail, excellent documentation practices, and ability to maintain audit-ready records. - Effective communication and interpersonal skills; ability to collaborate with cross-functional teams and external vendors. - Proficient with MS Office (Word, Excel, PowerPoint); experience with SAP and electronic quality management systems (Reliance, Veeva) preferred. Preferred Qualifications - Experience leading or supporting method transfers and performing go-sees. - Strong project coordination skills and ability to work with cross-functional teams. - Experience with implementation of LIMS. - Excellent written and verbal communication skills. Physical and Work Environment - Primarily office-based with occasional travel between sites. - Ability to travel for site visits/go-sees as required. Required Skills - Adaptability - Good Manufacturing Practices (GMP) - Laboratory Information Management System (LIMS) - Laboratory Operations - Manufacturing - Manufacturing Environments - Project Coordination - Quality Control (QC) - Quality Control Management - Quality Standards - Technical Transfer - Testing - USDA Regulations Preferred Skills - Laboratory Quality Control - Quality Management - Quality Management Systems (QMS) Benefits - Comprehensive package of benefits including medical, dental, vision healthcare and other insurance benefits (for employee and family). - Retirement benefits, including 401(k). - Paid holidays, vacation, and compassionate and sick days.