AI Deployment Strategist - Medtech R&D

Rematiq; Berlin; On-site; EUR 90,000 - 130,000; Full time

Benefits offered by this job

Equity

High-growth environment

Cross-functional exposure

Job summary

REMATIQ is shaping medtech R&D by building an AI platform for regulated workflows. We seek a Medtech R&D Domain Expert to help customers translate complex product development into practical AI-powered solutions.

You will work hands-on with customers, leading discovery, design workflows, and collaborating with R&D, Quality, Regulatory, and cross-functional teams to drive high-impact outcomes. English fluency is required; German is a strong plus.

Qualifications

• Extensive medtech R&D experience in regulated environments.
• Ability to translate workflows into AI-enabled use cases and deliverables.
• Strong client-facing communication and project management skills.

Responsibilities

• Own and drive customer project workstreams from discovery through delivery.
• Collaborate with R&D, Quality, Regulatory and cross-functional teams.
• Translate domain knowledge into practical AI-powered solutions and outputs.
• Create and review customer workshop materials and workflow maps.
• Incorporate customer feedback into internal product and engineering workflows.
• Actively use AI tools to speed up work and improve deliverables.

Skills

Medtech R&D domain expertise

Project ownership

Customer-facing communication

Hands-on execution

AI savviness

English fluency

German language

Job description

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.

We work with leading life sciences and medtech companies to help them move faster while improving quality, traceability, and compliance. We are looking for a Medtech R&D Domain Expert to help our customers transform complex product development workflows into practical AI-powered solutions.

What you’ll do

As a Medtech R&D Domain Expert at REMATIQ, you will work closely with customers, Delivery, Product, and Engineering to drive customer projects, create an understanding how medtech R&D 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 R&D, Quality, Regulatory, and cross‑functional customer teams to understand their product development processes, documentation, constraints, pain points, and opportunities for AI‑powered improvement.

• Bring domain expertise across medtech R&D workflows such as systems engineering, design controls, requirements, risk management, verification & validation, design reviews, design transfer, DHF / technical documentation, and related quality processes — and act as a domain sparring partner for internal teams.

• Create and review project deliverables such as customer workshop materials, R&D 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 medtech R&D domain 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 R&D, product development, innovation, design controls, technical project management, R&D transformation, or a related consulting role.

• Practical understanding of how medical devices are developed in regulated environments — including topics such as design controls, requirements management, risk management, verification & validation, design reviews, design transfer, DHF / technical documentation, and quality processes — and the ability to translate this 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 R&D, Quality, Regulatory, 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.

• Comfortable with speed and change: REMATIQ is growing extremely fast, with the organization doubling every 9‑12 months. You need to be comfortable in a high‑speed, high agency environment with rapidly changing scope and roles.

• 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 one of Europe’s fastest‑growing AI companies 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.

• Unmatched exposure: Work directly 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.