• Work as a QA Analyst / QA Tester

• Assist in conducting manual and automated penetration tests on web application and APIs to identify security vulnerabilities (OWASP Top 10). • Help assess the security of AI-driven features and LLM implementations, checking for vulnerabilities like prompt injection, data poisoning, insecure output handling, and model denial of service (OWASP Top 10 for LLMs). • Safely demonstrate the impact of discovered vulnerabilities by creating clear Proof-of-Concept (PoC) exploits. • Write comprehensive, technical security reports detailing findings, exploitation paths, risk ratings, and actionable remediation steps for development teams. • Work closely with software engineers to explain security flaws and guide them on secure coding best practices and remediation verification.

• Serve as a subject matter expert in benefit configuration and quality assurance across MedImpact’s PBM programs. • Lead complex validation efforts, oversee quality and compliance review activities, and ensure that configuration, operational processes, and deliverables meet client requirements and internal quality standards. • Drive continuous improvement, mentor analysts, and partner cross-functionally to enhance accuracy, efficiency, and compliance across the organization. • Lead the design, execution, and oversight of complex configuration validation activities for benefit, pharmacy network, and formulary administration in pre‑production environments. • Validate configuration accuracy for maintenance of business, new client implementations, regulatory updates, and special projects. • Approve configuration design plans for complex or unique benefit requests and ensure accurate migration of validated changes from Test to Production environments. • Communicate significant issues, risks, and improvement opportunities to leadership, ensuring visibility and timely resolution.

• Lead and implement product development, including the application of design controls, for new products and existing product changes including line extensions. • Create and maintain the design history file (DHF), including development of related specifications such as user requirements and design specifications. • Plan, implement, and report on design verification and validation studies, including bench and pre-clinical test protocols and reports. • Lead the development of manufacturing documentation and manufacturing process validation activities. • Responsible for risk management activities from product concept through commercialization. • Partner with Regulatory to support submissions for pre-market authorizations in the US. • Work closely with contract manufacturers and other suppliers to implement new projects and ensure supply chain meets performance and quality requirements. • Perform lot release, including reviewing batch records, device history records (DHRs), and process documentation for accuracy and completeness. • Support the intake, evaluation, and documentation of nonconforming materials. • Support post-market phase including product complaint handling, risk management, and post-market surveillance activities. • Help conduct supplier qualification and performance evaluation activities. • Communicate quality issues to suppliers and support resolution tasks. • Assist with internal audits and support external audits and inspections (e.g., FDA, ISO).