AI Deployment Strategist – MedTech Regulatory Affairs

About the Position

AI Deployment Strategist – MedTech Regulatory Affairs

Berlin

About REMATIQ

REMATIQ is revolutionizing how MedTech teams develop, document, and launch medical devices by building a highly specialized AI platform for regulated R&D, quality, and regulatory workflows.

We collaborate with leading life sciences and MedTech companies to help them accelerate while enhancing quality, traceability, and compliance. We are seeking an AI Deployment Strategist, MedTech Regulatory Affairs to assist our customers in transforming complex regulatory workflows into practical AI-powered solutions.

We value in-person collaboration and operate in a hybrid setup, with the team gathering in our office in the heart of Berlin-Mitte typically four days per week.

Responsibilities

As an AI Deployment Strategist, MedTech Regulatory Affairs at REMATIQ, 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.

Requirements

• 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, synthesizing findings, adapting to changing priorities, and driving work forward yourself.
• Comfort with speed and change: REMATIQ is growing extremely fast, with the organization 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.

We Offer

• 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.

About the Company

REMATIQ is changing how MedTech teams develop, document, and launch medical devices by building a highly specialized AI platform for regulated R&D, quality, and regulatory workflows.