• Design, implement, and continuously improve the automation framework for our products within an agile setup • Develop and maintain back-end integration tests using Java Spring and JUnit • Create and support integration testing with Cucumber, including guidance for team members • Build and execute front-end integration tests with Playwright • Collaborate closely with international teams across North America and Europe

• Plan and execute penetration tests (black box, gray box and white box) against web and mobile applications, APIs, internal/external networks and cloud environments. • Perform social engineering, phishing simulations and Red Team exercises when applicable. • Document findings in clear technical and executive reports, including evidence, risk classification (CVSS) and remediation recommendations. • Track and validate the remediation of vulnerabilities with development and infrastructure teams, performing retests as needed. • Provide complementary support to Threat Intelligence activities, including: • Monitoring and analysis of data leaks. • Analysis and investigation of phishing campaigns. • Execution and follow-up of takedown processes (removal of malicious domains, pages and content). • Mentor junior and mid-level analysts, contributing to the team’s technical development. • Stay up to date on new attack techniques, CVEs, TTPs (MITRE ATT&CK) and threat landscape trends.

• Prepare test environments for access control solutions, configuring systems, devices and rules required to validate scenarios. • Execute manual tests including functional, operational, exploratory, regression and integration tests, considering real-world usage scenarios involving software, hardware and business rules. • Develop and maintain test automation to support recurring validations, including APIs, interfaces, access rules, logs and events. • Use AI tools to increase productivity in the QA process, supporting the creation of scenarios, test cases, documentation, log analysis and generation of test data. • Validate integrations with equipment such as controllers, turnstiles, barrier gates, facial readers, biometric devices and RFID readers, ensuring proper communication, synchronization and event recording. • Log, classify and track bugs, documenting evidence, reproducing failures and validating fixes with technical teams. • Support approvals and work in partnership with product, development, deployment and project teams.

• Serve as the QA lead for assigned GMP-related activities including quality oversight of CDMOs, tech transfer, scale-up, manufacturing (cell bank, DS, DP, FDP), and disposition of clinical materials • Quality reviewer and approver for quality records such as change controls, CAPAs, deviations, temperature excursions, product complaints, expiry/retest, stability protocols/reports, master batch records, method qualifications, etc. • Collaborate with CMC, Supply Chain, Analytical Development and Program Management to ensure on-time delivery of products and compliance with all relevant cGMP regulations and guidelines as they pertain to manufacturing and supply operations • Supports archival of documents/records, quality metrics and develop/maintain QA related tracking logs • Work directly with operating entities (internal and CMOs) to ensure that product(s) meet all required quality standards and specifications • Supports management of Quality Agreements, including project coordination, cross-functional review, and approval workflows • Represent the Quality function in product development (CMC) teams to provide proactive quality guidance and decisions • Influence other functional departments to ensure that CMOs achieve and maintain the appropriate levels of GMP compliance and provide the highest level of quality services to Jade • Lead quality risk management activities to proactively identify, assess, and mitigate GMP-related risks across manufacturing and supply operations • Facilitate resolution of quality issues with internal and external parties in a timely manner • Coordinate communications with CMOs and internal technical product teams on quality issues • Review CMC sections of regulatory filings, as needed • Collaborate cross-functionally with CMC, Regulatory, Clinical Supply Chain, and Program Leadership teams to ensure quality is embedded across development and manufacturing activities • Participate in and support regulatory authority inspections and internal audits • Supports development/maintenance of Quality SOPs • Contribute to the development and maintenance of a positive team-focused company culture • Other duties, as assigned