Profile & Background
đź”— Connector profile grounded in pharmacy, industry, and structured development towards MedTech, regulation, and healthcare practice.
Language / Sprache / Sprog
English (current) · Deutsch – Profil & Hintergrund · Dansk – Profil & baggrund
👤 How this page fits into my connector role
This page outlines the professional background and patterns of thinking that form the basis of my developing connector role between medical technology, regulatory affairs, quality management, and practical healthcare workflows. It shows how experience from pharmacy, industrial contexts, and management supports a structured, process‑oriented way of working.
The focus is on the foundations: where I come from, how I approach complexity, and how this translates into my current development path in MedTech, regulation, quality, and AI in healthcare.
🏥 Professional background
Foundations in pharmacy and healthcare‑related work
My professional path started close to patients, medication processes, and everyday healthcare:
- Pharmaconomist (Denmark) – direct insight into pharmacy workflows, dispensing processes, and patient‑facing routines.
- Industrial supervisor in pharmacy – responsibility for structures, processes, and operational quality in pharmaceutical environments.
This experience provides a concrete understanding of how healthcare and pharmaceutical processes work in practice, with real constraints, risks, and organisational realities.
Extension into industrial and business contexts
Over time, I expanded into industrial and management‑oriented roles:
- Technical Business Economist – business and management perspective on technical and healthcare‑related environments.
- Work shaped by process thinking, quality orientation, and economic awareness.
This combination grounds my connector role in both operational detail and structural, organisational thinking.
đź“š Current development: MedTech, regulation, quality, AI in healthcare
I am deliberately building on this foundation in four interconnected areas.
MedTech regulatory affairs
- understanding how regulatory frameworks apply to medical technology products and processes
- linking requirements to concrete workflows, responsibilities, and documentation
- keeping the focus on clarity and practical usability for the people who work with them
Quality and risk management
- working with concepts oriented towards ISO 13485 and ISO 14971
- thinking in terms of processes, roles, and documentation
- treating standards as frameworks that need to be translated into everyday work, not as abstract checklists
AI in healthcare
- assessing how AI‑related approaches fit into regulatory and quality structures
- considering risk, accountability, and integration into existing healthcare and MedTech workflows
- aiming to place AI within stable, transparent frameworks
Regional focus: DE–DK–SE in a European context
- focusing on Germany, Denmark, Sweden, the wider German‑speaking region, and the European regulatory environment
- observing how expectations and structures differ between these contexts
- using these differences as input for connector work rather than treating them as isolated realities
🧠How I think and work
Analytical and structured approach
My default way of working is to:
- break complex topics into clear components
- identify relationships and dependencies
- build structured overviews before suggesting solutions
This supports traceable decisions and reduces noise in environments where regulatory affairs, quality management, and operational work intersect.
Process and quality orientation
I tend to think in terms of:
- stable processes instead of one‑off actions
- clearly defined roles and responsibilities
- documentation that supports both compliance and understanding
This aligns naturally with quality and risk‑based approaches in MedTech and healthcare.
Interdisciplinary perspective
I aim to connect:
- technical perspectives
- regulatory and quality demands
- operational workflows
- organisational and economic considerations
This helps prevent one dimension (for example purely technical or purely regulatory) from dominating in a way that creates problems elsewhere.
🧩 Connector identity in development
Step by step, I am shaping a connector role between medical technology, regulation, quality, and real‑world practice.
In practice, this often means:
- structuring open questions around regulation, quality, and processes
- organising information so that it becomes actionable and prioritised
- translating abstract requirements into workflows, responsibilities, and documentation
- paying attention to differences and interfaces between regions, especially DE–DK–SE
My connector role is grounded in practical experience and process thinking, not in abstract theory alone. The core of my profile is to structure complexity so that others can work with it in a clear, reliable way.
🎯 How this background supports my current work
This profile and background support my development as a connector between MedTech, regulatory affairs, quality management, and healthcare practice by:
- providing a realistic view of how healthcare and pharmaceutical work is actually done
- offering a process‑ and quality‑oriented mindset for structuring requirements
- enabling me to link regulatory, quality, and operational perspectives in a coherent way