Beschreibung

I am a PhD-level MedTech Product Manager, Technical Writer, and Clinical R&D Engineer specializing in driving complex medical devices through their entire lifecycle. With a deep technical foundation including a PhD in MRI and over 3 years of corporate experience at a global industry leader (Alcon), I seamlessly bridge the gap between rigorous biomedical engineering, regulatory compliance, and international commercial success.

I provide immediate, high-value B2B freelance support and consulting across Germany and Europe, focusing on:

• Medical Device Product Management & GTM Strategy: Portfolio management, owning the strategic roadmap, translating clinical user needs into technical requirements, and managing KOL relationships.

• Technical Writing & Regulatory Compliance: Preparing and optimizing technical documentation, clinical evaluation reports, and design verification protocols in strict compliance with MDR and ISO 13485 standards.

• Cross-Functional Leadership: Acting as the central operational interface to align R&D, Clinical Affairs, Regulatory, and Global Marketing teams across international boundaries.

• Specialized Domain Expertise: Advanced diagnostic imaging systems (MRI), ophthalmic diagnostics/surgical devices, and AI-driven Software as a Medical Device (SaMD).

Whether you are looking to unlock a stalled product roadmap, scale your digital health startup, or need senior hands-on support to clear an MDR compliance backlog, I am equipped to step into your project on Day 1 and deliver results.

Available for remote or hybrid contracts (based in Berlin). Let’s connect to discuss your project parameters.

Branchenexpertise

Sprachen

Englisch
Muttersprachlich oder zweisprachig

Arbeitsortpräferenzen

Vor Ort möglich

Berlin (bis zu 50 km)

Mitos
Product strategy and Growth Consultant
Mai 2026 - Heute (1 Monat)
Berlin, Germany
Partnering with leadership to scale operations, audit digital infrastructure, and streamline B2B product architectures. Designing and executing data-driven marketing and LinkedIn acquisition campaigns.
Business development Geschäftsbereichsstrategie Digitalisierung Product Development Wachstumsstrategie
VSY Biotechnology GmbH
Global Product Manager
BIOTECHNOLOGIE
August 2025 - Heute (10 Monate)
Berlin, Deutschland
Drove the international product lifecycle strategy, portfolio management, and cross-functional alignment for advanced ophthalmic medical devices. Acted as the central strategic interface between R&D, Clinical Affairs, Regulatory, and Global Marketing.

Key Responsibilities & Competencies:
• Product Lifecycle Management (PLM): Owned the strategic roadmap and lifecycle execution for premium ophthalmic diagnostics and surgical portfolio assets.
• Cross-Functional Leadership: Streamlined communication and project stage-gates across multidisciplinary international teams to accelerate timeline delivery.
• Go-to-Market (GTM) Strategy: Authored data-driven commercial strategies, competitive market positioning analyses, and product launch frameworks for the global market.
• Stakeholder & Clinical Interface: Collaborated closely with Key Opinion Leaders (KOLs), engineers, and clinicians to translate clinical user needs into clear technical requirements.
Product Lifecycle Management Stakeholder Management KOL management Cross-functional Team Leadership Public Speaking
AIRS Medical
Customer Success Manager
MEDIZIN
Juli 2024 - Januar 2025 (6 Monate)
Berlin, Germany
Managed clinical product adoption, post-market implementation, and high-level stakeholder relations for AI-driven diagnostic imaging software. Collaborated directly with clinical institutions and radiology departments to optimize product utilization and streamline workflows.

Key Responsibilities & Competencies:
• Product Adoption & Integration: Directed the seamless integration of complex AI software into existing hospital and radiology workflows, maximizing clinical user engagement.
• The R&D Feedback Loop: Acted as the vital link between clinical end-users and the core engineering teams, translating user friction and feature requests into technical product requirements.
• Clinical Stakeholder Management: Managed relationships with radiologists, chief medical officers, and hospital IT infrastructure leads, ensuring high product satisfaction and retention.
• Technical Writing & Training: Authored technical user documentation, onboarding frameworks, and product workflow guides to ensure compliant and scalable product deployment.
Stakeholder Management User-Testing Product Operations customer service DICOM