Medtech R&D Domain Expert

Meyandy LLC; Berlin; Hybrid; EUR 90.000 - 130.000; Vollzeit

Zusammenfassung

REMATIQ is building an AI platform for regulated R&D, quality, and regulatory workflows in medtech. We are seeking a Medtech R&D Domain Expert to help customers translate complex product development processes into practical AI-powered solutions.

You will own project workstreams from discovery to delivery, collaborate across R&D, Quality, and Regulatory teams, and turn domain knowledge into actionable outcomes. English fluency required; German a strong plus.

Qualifikationen

• 5–8 years of medtech R&D, product development, or related consulting experience.
• Practical understanding of regulated device development, design controls, risk management, V&V, and DHF.
• Ability to translate medtech workflows into AI-enabled use cases and deliverables.

Aufgaben

• Own and drive customer project workstreams from discovery through design, implementation, testing, and delivery.
• Collaborate with R&D, Quality, Regulatory, and cross-functional teams to understand processes and identify AI improvements.
• Translate domain expertise into practical AI use cases and structured product feedback for internal teams.
• Create and review workshop materials, workflow maps, gap analyses, and target designs with customer SMEs.
• Use AI tools to speed up work and improve project outputs.

Kenntnisse

Medtech R&D

Project ownership

Customer communication

Hands-on execution

AI-savvy

English fluency

German language

Jobbeschreibung

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.

• 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.

• 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 s… Medtech R&D Domain Expert — Rematiq Gmbh, Berlin.