Services
I support laboratories in structuring and implementing their processes within LIMS systems – with a focus on practical, traceable and regulatory-compliant solutions, particularly in pharmaceutical and similarly regulated environments.
Areas of support
Process Analysis and Structuring
Capturing and structuring existing laboratory processes as a basis for system implementation.
LIMS Workflow Development
Translating process logic into clear and practical LIMS workflows.
Configuration and Process Logic
Designing system logic, roles and process structures.
Permission Concepts
Developing appropriate role-based access models.
Legacy Data Migration
Structured transfer of data from legacy systems.
Validation-Oriented Support (CSV)
Support in validation-related activities with a focus on traceability and documentation.
Approach
I work in a structured, conceptual way with a strong focus on quality. Solutions are always considered in the context of laboratory reality, implementation feasibility and regulatory requirements.
This approach also shapes my role in project work and how I take responsibility and collaborate with stakeholders.
My role in projects
In projects, I take responsibility for the structured implementation of laboratory processes within LIMS systems while being closely integrated into project teams.
I gather requirements directly with domain experts, often on-site in the laboratory, and develop structured solutions ranging from workflows and master data to permissions and system configurations.
I work independently and actively contribute improvements, aligning larger changes with project stakeholders.
I collaborate closely with project managers, domain experts and key users, enabling sustainable system usage.
I also support user training and troubleshooting, and contribute to validation-related activities.
The following examples illustrate situations from past projects where I was involved.