Global Solution Engineer

🕒 Dezembro 25, 2025

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Docuvera

SiteLinkedInTodas as Vagas

51 - 200 funcionários

🏥 Saúde

💼 Consultoria

📦 Logística

Healthcare • Consulting • Logistics

A Docuvera é uma plataforma SaaS baseada em IA, pronta para validação, desenvolvida especificamente para organizações de ciências da vida reguladas, destinada a criar, gerenciar e publicar conteúdo estruturado e reutilizável. Ela centraliza componentes de conteúdo modular em todo o processo de rotulagem, CMC, informações clínicas, médicas, farmacovigilância/segurança e qualidade/SOPs para garantir conformidade regulatória (ex. : eCTD/ePI, 21 CFR Parte 11, Anexo 11), manter trilhas de auditoria e acelerar o tempo de lançamento no mercado. A plataforma enfatiza recursos de governança, controle de versões, metadados e hospedagem segura (SOC 2 Tipo II, ISO 27001) para atender às necessidades globais de documentação e submissão farmacêutica.

Descrição

• Serve as a critical bridge between commercial sales, customer success, and product teams. • Collaborate with Account Executives on discovery and business case development. • Engage with the Customer Success team to define readiness and scope post-sale. • Help prospects understand the strategic value of structured content platforms in regulatory and clinical use cases. • Lead architecture design sessions, mapping integration and content reuse strategies. • Participate in global workshops, industry events, webinars, and customer advisory activities.

🎯 Requisitos

• 7–12 years in Solution Consulting or Sales Engineering for B2B SaaS. • Regulatory Information Management or Digital Transformation within pharma. • Technical product management or implementation consulting. • Proven experience working with structured content platforms and/or traditional content management systems such as Veeva, OpenText, CARA. • Demonstrated success supporting large, global clients with complex regulatory and operational requirements. • Strong storytelling, communication, and executive presentation capabilities. • Ability to translate complex features into commercial, regulatory, and operational value. • Strong understanding of life sciences regulatory frameworks, including GxP, eCTD, IDMP, 21 CFR Part 11, EMA/FDA guidance. • Strong knowledge of FHIR standards as applied to pharmaceutical regulatory contexts, including ePI, ICH M11 technical specifications. • Proficient in building, configuring, and managing RESTful API transactions between enterprise SaaS platforms.

🏖️ Benefícios

• Work your way. We’re digital-first and fully flexible, with asynchronous work as the norm. • Pride in what we do. There's nothing like joining a tech scale-up that's highly regarded on the world stage where what we do makes a tangible difference in the world. • Modern tools that work for you. We use the latest systems, including AI, to make work smarter. • Space to grow. You’ll have access to learning and development resources. • A close-knit global team. You’ll be part of a dedicated, collaborative community that stays connected no matter where you’re based.