I am a Senior Technical Writer and have worked in technical documentation since 2015. The groundwork came earlier: from 2010, I worked on maritime safety documentation as a technical coordinator, in 2013 I completed six months of tekom training, and in 2014 I received my tekom certification as a technical writer.
Media, PR and marketing communication have been part of my work since 1994. From 1994 to 1996 and again in 2000, I worked in communication and PR for NGOs. From 1997, I worked for a broadcaster, and in 1998 I completed a journalism traineeship in TV editorial work and magazine program production. In 2000 and 2001, I worked on TV program development for the pan-Arab region.
In technical documentation, I have worked for machinery, MedTech and other regulated technical environments. My work covers information architecture, technical documentation, CE coordination, machine safety, safety-related product information, risk assessment and regulatory documentation. In MedTech, this meant working not only with the Medical Device Regulation (MDR) but also with the requirements of the US Food and Drug Administration (FDA) and of China’s National Medical Products Administration (NMPA). I have supported MDR certifications.
My editorial background — journalism, storytelling, e-learning formats, and video and TV production — complements my work in technical communication; it is not its foundation. The principles of tekom and of technical communication differ considerably from editorial TV work: structure, unambiguous instructions and safety-related information follow rules of their own. The editorial side adds attention to the reader, to sequence and to what an image can explain better than a paragraph. Today I bring both together in microlearning formats and micro-videos on technical and regulatory topics.
As a publisher and editor, I publish articles and analyses on AI TechDoc Press and contribute to AI TechDoc Knowledge, where blueprints, context cards and a preview of the AI learning path are available. My two LinkedIn newsletters, “Cut Complexity — Create Clarity” and “Write it Safe. Prove it Safe.,” and the case notes on Technical Documentation Expertise show how I work on real topics.
- Documentation systems
- XML-based environments, including SCHEMA ST4, FrameMaker and Sirius CMS
- Standards and regulations in my work
- Machinery Directive 2006/42/EC, Machinery Regulation (EU) 2023/1230, ISO 12100, ISO 13849, IEC 62061, IEC/IEEE 82079-1, Medical Device Regulation (MDR), FDA requirements for medical devices (USA), NMPA requirements for medical devices (China)
- Formats
- Operating manuals, safety-related product information, regulatory documentation, microlearning, micro-videos, editorial and PR texts
- Industries
- Machinery and automated production lines, robotics, medical technology (including in-vitro diagnostics and radiology), pharmaceutical production (GMP), rail vehicles, maritime and naval shipbuilding, photonics and optics, semiconductors and electronics, industrial software and automation
- Subject areas
- Photonics and optics: optical measurement, sensor and imaging systems, metrology, NIR · Semiconductors: integrated circuits, data sheets, motion control with stepper motors and drives · Robotics and automation: robot arms, networked production lines, PLC-controlled interfaces, HMI, safety functions · Mechatronic systems · X-ray and fluoroscopy · Medical device software · GMP and data integrity (ALCOA+)