• Diseñe, desarrolle y ejecute scripts de prueba automatizados utilizando herramientas de automatización estándar de la industria. • Colaborar con equipos multifuncionales para comprender los requisitos de software y desarrollar planes de prueba. • Identificar, documentar y realizar un seguimiento de los defectos e inconsistencias del software. • Realice pruebas de regresión exhaustivas cuando se resuelvan los errores. • Analizar los resultados de las pruebas y proporcionar informes detallados al equipo de desarrollo. • Manténgase actualizado con las últimas tendencias y tecnologías de la industria en pruebas y automatización de software. • Mejorar y optimizar continuamente el proceso de pruebas de automatización.

Role Description We are seeking a highly skilled Test Staff Engineer with deep expertise in Firewall/Security testing and strong hands-on automation. This role requires technical leadership, end-to-end ownership of test strategy for assigned components, and building scalable automation and test tools to ensure high-quality SonicOS releases. Key Responsibilities - Own test strategy, planning, execution, and quality sign-off for SonicOS components - Architect, develop, and maintain automation frameworks, pipelines, and test tools - Drive an automation-first regression strategy and improve overall test coverage - Perform complex system, integration, and upgrade/downgrade testing - Partner with Dev/PM in design reviews, scrums, and defect triage - Lead root-cause analysis and validation of critical customer issues - Mentor engineers; review test plans, automation design, and coverage - Drive release readiness, escape analysis, and quality metrics Qualifications - Strong Networking: TCP/IP, Routing, NAT, VLANs, Firewall policies - Firewall/Security: VPN, DPI/App Control, IPS, Gateway AV, Geo-IP, Botnet - Automation: Playwright / Selenium / PyTest / Robot Framework - Programming: Python or JavaScript (framework/tool development) - Linux/Unix, debugging with logs, core dumps, packet capture (tcpdump/Wireshark) - CI/CD integration (Jenkins, Git-based pipelines) - Defect tracking & test management (JIRA or similar) - Exposure to effective usage of AI tools Requirements - Experience with signature-based services & live update pipelines - Cloud test environments (AWS/Azure) - Handling customer escalations/field issue reproduction Soft Skills - Technical leadership, strong ownership, and decision-making - Excellent debugging and communication skills - Ability to lead quality initiatives across teams Education - B.E / B.Tech / M.Tech in CS/IT or related fields Company Description SonicWall is a cybersecurity forerunner with more than 30 years of expertise and is recognized as a leading partner-first company, ensuring our partners and their customers are never alone in the fight against cybercrime. For more information, visit www.sonicwall.com or follow us on Twitter , LinkedIn , Facebook , and Instagram .

• Own QA for each release from start to production • Master end-to-end user flows • Identify: Edge cases, Logical inconsistencies, UX issues, Technical or data-related risks • Challenge product and UX choices when necessary • Structure and prioritize QA feedback for developers • Collaborate closely with the CTO during iterations • Help define a solid QA approach even with incomplete specs

QA Regulatory Data SME US - Remote (Any location) Full time 40882 Job Family: Data Science & Analysis Travel Required: Up to 10% Clearance Required: Ability to Obtain Public Trust Our federal client conducts product testing, quality evaluations, and risk assessments to support market interventions and ensure pharmaceutical manufacturing quality. The associated data repository serves as a critical system of record underpinning regulatory decision-making for pharmaceutical products. This role supports an internal audit of drug quality sampling and testing databases to ensure data integrity, regulatory compliance, and methodological consistency. The SME will assess data quality, validate adherence to FDA standards, and provide actionable recommendations to strengthen regulatory decision-making processes. What You Will Do: - Perform comprehensive reviews of database records to evaluate completeness, accuracy, and consistency - Analyze variations in sampling and testing procedures and assess impacts to data quality and integrity across data sources. - Assess compliance of documentation and data controls with FDA regulations, guidance, and standard operating procedures - Evaluate completeness, and consistency and gaps in supporting documentation associated with testing activities - Identify deviation, inconsistencies from established processes and risks impacting regulatory decisions; - Provide prioritized, actionable recommendations for corrective and preventive actions (CAPA) - Support alignment of database practices with regulatory expectations and audit standards - Prepare a comprehensive final audit report detailing observations, risk areas, and root causes - Present findings and recommendations to stakeholders across regulatory, scientific, and program leadership teams - Support implementation planning for process improvements and data governance enhancements What You Will Need: - Bachelor’s Degree in Chemistry, Pharmaceutical Sciences, Regulatory Science, Data Science, or related discipline - Minimum five (5) years of relevant experience in regulatory data analysis, quality assurance, or FDA-regulated environments - Demonstrated ability to define problems and analyze complex systems within regulatory or scientific domains - Experience developing analysis plans, evaluating data quality, and supporting regulatory decision-making processes - Experience coordinating and managing analytical evaluations, audits, or compliance reviews - Strong knowledge of FDA regulations, data integrity principles (e.g., ALCOA+), and laboratory documentation standards - Ability to assess system specifications and recommend improvements for implementation - Excellent written and verbal communication skills, including status reports, technical reports and audit documentation - Strong critical thinking and problem-solving capabilities in complex regulatory environments - Hybrid role requiring the ability to work onsite at the client location in Silver Spring, MD What Would Be Nice To Have: - Advanced degree (Master’s or PhD) in a relevant scientific or regulatory discipline - Experience supporting regulatory quality surveillance initiatives, data systems and data management practices. - Familiarity with drug quality sampling, laboratory testing workflows, and analytical validation processes. - Experience conducting internal audits or supporting regulatory inspections (e.g., FDA, ISO, GLP). - Knowledge of database systems used for laboratory data management (e.g., LIMS), scientific instruments and laboratory equipment. - Experience with data governance, quality frameworks, and process improvement methodologies. - Experience translating audit findings into operational and system-level improvements The annual salary range for this position is $85,000.00-$141,000.00. Compensation decisions depend on a wide range of factors, including but not limited to skill sets, experience and training, security clearances, licensure and certifications, and other business and organizational needs. What We Offer: Guidehouse offers a comprehensive, total rewards package that includes competitive compensation and a flexible benefits package that reflects our commitment to creating a diverse and supportive workplace. Benefits include: - Medical, Rx, Dental & Vision Insurance - Personal and Family Sick Time & Company Paid Holidays - Parental Leave - 401(k) Retirement Plan - Group Term Life and Travel Assistance - Voluntary Life and AD&D Insurance - Health Savings Account, Health Care & Dependent Care Flexible Spending Accounts - Transit and Parking Commuter Benefits - Short-Term & Long-Term Disability - Tuition Reimbursement, Personal Development, Certifications & Learning Opportunities - Employee Referral Program - Corporate Sponsored Events & Community Outreach - Care.com annual membership - Employee Assistance Program - Supplemental Benefits via Corestream (Critical Care, Hospital Indemnity, Accident Insurance, Legal Assistance and ID theft protection, etc.) - Position may be eligible for a discretionary variable incentive bonus