Global Solution Engineer

🕒 December 25, 2025

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Docuvera

WebsiteLinkedInAll Job Openings

51 - 200 employees

💊 Pharmaceuticals

☁️ SaaS

📋 Compliance

Pharmaceuticals • SaaS • Compliance

Docuvera is an AI-powered, validation-ready SaaS platform purpose-built for regulated life sciences organizations to author, manage, and publish structured, reusable content. It centralizes modular content components across labeling, CMC, clinical, medical information, pharmacovigilance/safety, and quality/SOPs to ensure regulatory compliance (e. g. , eCTD/ePI, 21 CFR Part 11, Annex 11), maintain audit trails, and accelerate time to market. The platform emphasizes governance-first features, version control, metadata, and secure hosting (SOC 2 Type II, ISO 27001) to support global pharma documentation and submission needs.

📋 Description

• 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.

🎯 Requirements

• 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.

🏖️ Benefits

• 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.