--- title: "AI Deployment Strategist – MedTech Regulatory Affairs" company: "Rematiq GmbH" company_url: "https://www.remjobs.works/companies/rematiq-gmbh" url: "https://www.remjobs.works/job/rematiq-gmbh-ai-deployment-strategist-medtech-regulatory-affairs-010f6c16-d706-448d-bc50-fa080337c110" apply_url: "https://jobs.ashbyhq.com/rematiq-gmbh/1c0615c5-ad2e-4704-b8f8-91129d1bcc45" workplace: onsite location: "Berlin" employment_type: full-time seniority: mid role: ai-machine-learning region: europe date_posted: 2026-08-21T18:01:47.557Z first_seen_by_remjobs: 2026-09-19T22:08:09.240Z --- # AI Deployment Strategist – MedTech Regulatory Affairs **Rematiq GmbH** · Berlin Apply: https://jobs.ashbyhq.com/rematiq-gmbh/1c0615c5-ad2e-4704-b8f8-91129d1bcc45 ## About the role #### About REMATIQ REMATIQ is changing how MedTech teams develop, document, and launch medical devices by building a highly specialised AI platform for regulated R&D, quality, and regulatory workflows. We work with leading life sciences and MedTech companies to help them move faster while improving quality, traceability, and compliance. We are looking for an **AI Deployment Strategist, MedTech Regulatory Affairs** to help our customers transform complex regulatory workflows into practical AI-powered solutions. We believe in the value of in-person collaboration and work in a hybrid setup, with the team coming together in our office in the heart of **Berlin-Mitte** typically **four days per week**. #### What you’ll do As an **AI Deployment Strategist, MedTech Regulatory Affairs** at REMATIQ, you will work closely with customers, Delivery, Product, and Engineering to drive customer projects, understand how MedTech regulatory teams work today, and help translate these workflows into high-impact AI use cases. This is not an academic advisory role. You will be hands-on in customer projects, helping structure problems, drive workstreams, create materials, review outputs, and turn domain expertise into practical solutions. You will: - Own and drive customer project workstreams from discovery through workflow design, implementation support, testing, iteration, and delivery. - Work directly with Regulatory Affairs, R&D, Quality, and cross-functional customer teams to understand regulatory submissions, regulatory intelligence and compliance workflows, product development processes, documentation, constraints, pain points, and opportunities for AI-powered improvement. - Bring deep MedTech Regulatory Affairs expertise across areas such as regulatory strategy and intelligence, submissions, compliance, design assurance, audits, and interactions with adjacent R&D and quality processes — and act as a domain sparring partner for internal teams. - Create and review project deliverables such as customer workshop materials, workflow maps, gap analyses, impact assessments, target process designs, use-case specifications, and AI-generated outputs together with customer subject-matter experts. - Collect customer learnings and feedback and translate them into structured internal feedback for Product and Engineering. - Use AI tools actively to speed up your own work, create high-quality outputs faster, and improve how customer projects are delivered. #### What we’re looking for We are looking for someone who combines deep MedTech Regulatory Affairs expertise, strong project ownership, customer-facing communication, and a hands-on execution mindset. You may be a strong fit if you have: - 5–8 years of relevant experience in MedTech Regulatory Affairs, regulatory strategy, regulatory operations, design assurance, or a related consulting role. - Practical understanding of how medical devices move through regulated development and regulatory pathways, including areas such as regulatory strategy, submissions, design controls, requirements and risk management, verification & validation, design reviews, audits, and technical documentation — and the ability to translate this expertise into AI-enabled use cases, project deliverables, and structured product feedback. - Strong project ownership: you can structure ambiguous work, align stakeholders, manage risks, define next steps, and drive cross-functional customer projects from problem understanding to delivery. - Strong customer-facing communication: you can build trust with Regulatory Affairs, R&D, Quality, and senior stakeholders, ask sharp questions, and explain complex topics clearly. - Hands-on execution mindset: you are comfortable creating materials, mapping workflows, reviewing outputs, synthesising findings, adapting to changing priorities, and driving work forward yourself. - Comfort with speed and change: REMATIQ is growing extremely fast, with the organisation doubling every 9–12 months. You are comfortable operating in a high-speed, high-agency environment with rapidly changing scope and responsibilities. - AI savviness: you actively use AI tools to improve your own work, move faster, create better deliverables, and explore new ways of working. - Fluency in English; German is a strong plus for German-speaking customer work. #### Why join REMATIQ? - Rare timing: Join REMATIQ at a pivotal stage as we move from Seed toward Series A and prepare to significantly grow the team. - Real ownership: Own high-impact customer projects and see your work translate directly into outcomes for leading MedTech and life sciences companies. - Direct exposure: Work closely with founders, customers, product teams, and technical experts while building a network across the global MedTech and life sciences industry. - Purposeful work: Be part of a mission-driven team transforming how medical devices reach the market — in an industry where quality, compliance, and patient safety mean nothing can be left to chance. - Compensation & growth: Competitive salary plus equity, giving you a stake in the success you help create. --- Source: Rematiq GmbH's own career page, read by RemJobs. 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