• Your task includes evaluating and providing feedback by using a set methodology. • In addition, you need to determine whether the content sourced to you contains any objective errors. • All information regarding the quality of the content has to be filled in a specific report. • You will be in touch with a project manager who will provide guidelines and support through the process.

• Working independently and collaboratively with a team to both lead and support • Perform penetration testing on applications with complex technology stacks from both a: Blackbox & Whitebox perspective • Dynamically flex your skills when assessing emerging or custom technologies • Contextualize vulnerabilities and assess realistic impact to a client accounting for mitigating and aggravating factors • Manage priorities and tasks to achieve utilization targets • Operate with professionalism both internally and with clients • Ensure quality reports and services are delivered efficiently and on time • Maintains strong depth of knowledge in the practice area • Collaborate with project managers, quality management, sales and other delivery team members to drive customer satisfaction and meet project deliverables • Up to 10% travel

• Be an important part of the QA Testing process for emerging technology • Test never before seen apps/technology, e-courses, marketing materials, or other interesting tasks • Follow written testing instructions in English

• Serve as a clinical and technical subject matter expert within Quality Assurance and provides advanced clinical expertise to assess device performance concerns, determine regulatory reportability, identify root causes, and support risk management activities. • Partner closely with Field Clinical and Technical teams to ensure timely reporting of device-related issues and collection of complete, high-quality information to support thorough complaint investigation and evaluation. • Act as senior clinical and technical SME for complaint investigations involving implantable medical devices including assessment of device performance and patient outcomes. • Provide expert clinical and technical analysis to support root cause determination, including differentiation between device-related, use-related and patient specific factors. • Support Quality Leadership in identifying emerging product performance trends, reliability concerns, and potential risk signals through complaint trending and data analysis. • Perform global regulatory reportability assessments in accordance with applicable regulations, including FDA Medical Device Reporting (21 CFR 803), EU MDR Vigilance Reporting, TGA, PMDA, MHRA, and other international regulatory requirements. • Serve as Clinical Quality SME supporting cross-functional collaboration across Quality, Regulatory Affairs, R&D, Manufacturing, and Clinical teams.