• Arquitetar e desenvolver workflows avançados no n8n, utilizando lógica complexa, Code Nodes (JavaScript) e manipulação de JSON. • Criar e manter integrações via Webhooks, garantindo comunicação bidirecional entre Strapi e serviços externos. • Consumir e integrar APIs REST e GraphQL (queries e mutations). • Implementar resiliência operacional: retries inteligentes, filas/rotas de erro, alertas e fallback. • Realizar tratamento, limpeza e transformação de dados, lidando com diferentes formatos e schemas. • Apoiar integrações no produto (Next.js), conectando fluxos técnicos à experiência do usuário.

• Develop and validate the manufacturing processes and workflow for composite parts • Assist in the design for tooling and fixtures required for manufacturing aerospace components • Generate manufacturing bill of materials as required for the program • Review drawings and 3D models to ensure they meet design intent • Coordinate with external suppliers to ensure deliverables are met on schedule • Troubleshoot manufacturing issues that arise during development and lead root cause corrective actions • Create process plans and work instructions for each component or system, ensuring the product is in compliance with standard aerospace quality standards • Support manufacturing production planning and coordination, capacity planning, line design, production execution, and operations process development • Disposition non-conforming parts, identify root cause, and implement corrective and/or preventive actions to reduce scrap and rework • Perform continuous improvement to improve yield and reduce production costs • Perform design reviews and provide technical input related to dynamic systems, assisting in the selection of manufacturing methods, materials, and quality and inspection requirements • Establish and enforce best practices for critical aerospace components

• Designs, develops, validates, and/or debugs software abstractions and frameworks for acceleration with FPGAs to support embedded, data center, and communication clients. • Collaborate with architects and design engineers to understand IP specifications and define comprehensive verification strategies and detailed test plans. • Develop robust, reusable, and constrained-random verification environments using SystemVerilog and UVM (Universal Verification Methodology). • Create and implement directed and random test cases and test sequences to exercise design functionality and uncover potential bugs. • Develop verification components, including drivers, monitors, scoreboards, and checkers. • Utilize SystemVerilog Assertions (SVA) and formal verification methods to enhance bug detection and verify complex properties. • Execute simulation regressions, debug test failures, analyze root causes, and work with designers to implement corrective measures. • Define and track functional and code coverage metrics to ensure verification completeness and drive coverage closure. • Develop automation scripts and infrastructure using languages like Python or Perl to improve verification efficiency and flows. • Participate in technical reviews of specifications, design documents, and test plans, providing valuable input and feedback.

• Serve as the **HFE lead for the contract**, owning the HFE strategy, roadmap, and quality bar for deliverables; establish HFE governance, definitions of ready/done, templates, and review gates. • Translate **state‑of‑the‑art research and industry trends** in human factors, cognitive/organizational psychology, and clinical informatics into scalable methods and guidance for teams. • Champion **Lean‑Agile** principles within a SAFe® environment, shaping ART ceremonies (PI Planning, System Demo, Inspect & Adapt) to drive value delivery and continuous improvement. • Plan and execute **mixed‑methods research** (contextual inquiry, cognitive task analysis, diary studies, think‑aloud protocols, surveys, card sorting, tree testing, formative/summative usability) tailored to risk and regulatory context. • Design and conduct **workflow analyses** across clinical informatics domains (e.g., order entry, medication administration, care coordination, documentation, decision support) to identify **latent conditions**, handoff risks, and transient failure modes that **evade unit testing**. • Apply advanced **risk and resilience methods** (e.g., FMEA/FMECA, STPA, bow‑tie analysis, FRAM, HFACS) to anticipate and mitigate human‑system hazards. • Visualize and articulate **system‑wide impacts** of design changes on **all user groups** (end users, supervisors, support staff, patients, administrators). • Recommend **redesigns** or **operational mitigations** to minimize negative outcomes when changes are constrained or products/processes are essential. • Collaborate with product, engineering, clinical SMEs, and data teams to prototype designs (low‑ to high‑fidelity) and evaluate effects on safety, workflow, workload, and adoption. • Provide **thoughtful, actionable suggestions during live demo calls**; adapt in real time to participant feedback in user sessions of any type (moderated, unmoderated, remote, in‑person). • Mentor cross‑functional teams in HFE practices; deliver trainings and brown‑bag sessions to **empower high‑performing Agile teams**. • Define and track **HFE KPIs** (e.g., task success, time‑on‑task, error rates, cognitive load, adoption, defect escape rate, alert fatigue indices). • Produce clear, standards‑aligned HFE documentation (protocols, moderation guides, test plans, risk analyses, traceability matrices, usability engineering files, summative reports). • Ensure alignment with applicable **standards and guidance**