29.05.2026 aktualisiert

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Integration Architect – Laboratory & Manufacturing Systems | Requirements Engineer

Blaustein, Deutschland
Deutschland +2
info: Deutschland, Österreich, Schweiz
Dipl. Ing. FH
Blaustein, Deutschland
Deutschland +2
info: Deutschland, Österreich, Schweiz
Dipl. Ing. FH

Profilanlagen

02_CV_SHORT_DE.pdf
01_CV_LONG_DE.pdf
02_CV_SHORT_EN.pdf
03_CONSULT_EN.pdf
01_CV_LONG_EN.pdf
03_CONSULT_DE.pdf
2026_Südzucker-Beneo.pdf
2021_QIAGEN.Global.Engineering.pdf
2023_QIAGEN_Letter_Christoph_Speth.pdf
2026_Boehringer-Ingelheim_DigitalEnablement.pdf
2020_Boehringer.Ingelheim.Process.Science.pdf
2026_PRINCE2_Agile_Foundation.pdf
2026_Professional Scrum Master I.pdf
2026_KI-Consultant_01.pdf

Über mich

With 25+ years in software delivery, I combine technical depth with structured Requirements Engineering and Business Analysis. By connecting business, IT, and governance, I turn fragmented requirements into structured delivery models enabling informed decisions and sustainable implementation.

Skills

Data IntegrationRequirements EngineeringSystem Design
Positioning
Integration Architect and Digitalization Consultant specializing in laboratory systems, manufacturing data integration, and regulated environments (biotech, diagnostics, healthcare).
My Expertise
Senior technology consultant with more than 25 years of experience designing and implementing complex software and data integration systems in biotechnology, diagnostics, healthcare IT, and regulated manufacturing environments.
  1. Specialized in connecting laboratory systems, production equipment, and enterprise platforms into coherent digital architectures that enable traceability, quality insights, and operational efficiency.
  2. Combines requirements engineering, system architecture, and hands-on development, enabling projects to move efficiently from concept and stakeholder requirements to reliable production systems.
What I Help Organizations Achieve
  1. Connect laboratory instruments, production equipment, and enterprise systems into coherent digital platforms
  2. Transform fragmented laboratory and manufacturing data into structured, traceable information
  3. Design integration architectures that scale from pilot projects to production environments
  4. Translate complex scientific and operational workflows into robust digital systems
  5. Stabilize and modernize legacy laboratory or manufacturing IT landscapes
Typical Engagement Scenarios
  1. Laboratory digitalization initiatives
  2. LIMS architecture, migration, or modernization
  3. Manufacturing data platform design
  4. Integration of laboratory instruments and production systems
  5. Scientific workflow digitalization
Unique Value
Combines requirements engineering, system architecture, and hands-on implementation. This allows projects to move efficiently from stakeholder requirements and system design to reliable, production-ready software and integration solutions.

Sprachen

DeutschMutterspracheEnglischverhandlungssicher

Projekthistorie

Shop Floor OT - Business Analysis & Solution Development

QIAGEN

Pharma und Medizintechnik

>10.000 Mitarbeiter

  1. Business Analysis
  2. Implement control logic acting as a QC gate
  3. QA documentation (URS, SDS, Risk Matrix, IQ documents)
  4. Rollout

Business Analyst / Data Integration Consultant – Laboratory & Production Integration (Labware LIMS)

Südzucker/Beneo

Sonstiges

5000-10.000 Mitarbeiter

At Südzucker, I supported several initiatives related to the modernization and integration of laboratory systems in a GAMP-regulated food production environment.
A key focus was the migration of a LabWare LIMS (version 7) from an on-premise environment to the Azure Cloud, including the virtualization of laboratory clients and ensuring continued system operation in the new infrastructure.
In addition, I contributed to the integration of laboratory instruments and enterprise systems, and participated as the LIMS lead within an interdisciplinary project team during the construction of a new faba bean processing mill.
Responsibilities
  1. Contribution to the migration of LabWare LIMS v7 from on-premise to cloud infrastructure (Azure)
  2. Implementation of virtualized laboratory clients in the cloud environment
  3. Integration of Agilent HPLC systems into the LIMS landscape
  4. Development of SAP interfaces using SAP Cloud Platform Integration (CPI)
  5. Acting as LIMS lead within an interdisciplinary project team for a new faba bean mill
  6. Troubleshooting and operational support for laboratory and integration systems

Business Analyst / Developer

Boehringer Ingelheim

Pharma und Medizintechnik

>10.000 Mitarbeiter

  1. Business Analysis & User Requirements
  2. Migrations of several applications from APEX 5.0 to APEX 24.0
  3. Extend applications with new features
  4. Adaptions to ORACLE packages
  5. Framework for ORACLE scheduler with ORACLE job engine.

Integration Architect / Data Engineer – Manufacturing Data Platform

QIAGEN

Pharma und Medizintechnik

1000-5000 Mitarbeiter

As part of the modernization of QIAStatDx cartridge production, I worked as an IT/OT consultant and technical lead in a cross-functional engineering team, supporting the transition from isolated workstations to a connected manufacturing environment.
The objective was to transform fragmented workstation data (“Islands of Information”) into a connected production data ecosystem (“Connected Plant”) enabling traceability, quality insights and process optimization.
To achieve this, we designed and implemented a modular and validated data interface architecture integrating laboratory equipment, machine workstations and production systems.

QIAGEN is a global provider of molecular diagnostics. The QIAStatDx PCR platform enables simultaneous detection of multiple respiratory pathogens in a single test run.
Responsibilities
  1. Technical concept development and technical lead for data integration architecture
  2. Design and implementation of data-driven applications and dashboards
  3. Design and implementation of modular interfaces for production and laboratory systems
  4. Creation of validation documentation (URS, FDS, SDS, risk matrices)
  5. Execution of qualification activities (DQ, IQ, OQ, PQ)
  6. Coordination with equipment vendors and engineering teams
  7. Collaboration in a multidisciplinary team including data scientists, data engineers, process engineers and production supervisors
  8. Contribution in the grounding of a nearshore team
  9. Mentoring and onboarding of additional developers


Business Analyst / Software Engineer

QIAGEN

Pharma und Medizintechnik

1000-5000 Mitarbeiter

Global Engineering Biotechnology (QIAstat-dx Production Line)
  • Working in a team of engineers, data scientists, and data engineers for a PCR kit.
  • Requirements engineering with end users and stakeholders.
  • Coordinating software projects with solution providers.
  • Writing and executing GMP-relevant qualification documents (DQ / IQ / OQ / PQ).
  • Azure backend development for data analytics interfaces (.NET Core).
  • Frontend development of a QC platform (C# / ASP.NET Core / Razor / JavaScript).
  • Digitization of workstreams.
  • IPC data acquisition.
  • Configuration of proprietary shopfloor workstations (Panel PCs).

Software Engineer / LIMS Consultant

Boehringer Ingelheim

Pharma und Medizintechnik

>10.000 Mitarbeiter

Boehringer Ingelheim – LabWare LIMS for Process Science (Biopharma) Technical Consultant (2012–2019)
For Boehringer Ingelheim Process Science, I worked for 7 yrs. on the development of a LabWare LIMS supporting biopharmaceutical process development.
Process Science develops scalable manufacturing processes for biologics, covering Upstream Development (USD) for fermentation and Downstream Development (DSD) for purification. The LIMS environment supported experiment-driven research workflows, where scientists design, modify and evaluate experimental setups.
To support this environment, a high configurability and generic design, enabling administrators to model complex experimental workflows, without requiring constant software development was needed.
Although the system operated in a non-GMP R&D environment, it required robust data structures, traceability and high technical quality standards.
I worked in this setting across two Process Science sites (Biberach and Vienna) and played an active role in knowledge and concept transfer between the sites, helping to align system design, workflows and best practices.

Responsibilities
  1. Design and implementation of process templates for upstream and downstream experiments
  2. Implementation of technical integrations and generic data import mechanisms
  3. Analysis macros and laboratory automation extensions
  4. Migration from LabWare v6 to v7
  5. Use cases and concepts
  6. Training for LIMS system admins
  7. Concept transfer of sites Biberach and Vienna

Software Solution Provider

Thermo Fisher

Pharma und Medizintechnik

>10.000 Mitarbeiter

LIMS Implementation for Customer-Specific Peptide Production
Conception and implementation of a Laboratory Information Management System (LIMS) supporting the production of customer-specific peptides (“lot size one”).
At project start, peptide production relied on fragmented tools and largely manual workflows. In collaboration with scientists and production staff, the existing processes were analyzed and translated into a digitally integrated workflow and data model enabling structured data capture, traceability and cross-system integration.
A key aspect of the project was the digital transformation of laboratory and production processes, establishing a shared understanding of how peptide synthesis, purification and analytical workflows could be connected within a single information system.
Responsibilities
  1. Analysis of laboratory and production workflows through process reviews and stakeholder workshops
  2. Development of functional specifications and system concepts
  3. Data model and software architecture design
  4. Design and implementation of interfaces to the ERP system (Navision)
  5. Implementation of the LIMS application and workflow logic

Software Developer & Requirements Engineer

Meierhofer AG

Pharma und Medizintechnik

50-250 Mitarbeiter

For Meierhofer AG, a provider of clinical information systems, I worked for seven years as a software engineer, focused on .NET technologies, initially as an employee and later as a freelance consultant.
The work focused on the development and integration of modules for MCC.NET, a high-performance electronic patient record system used in clinical environments. My role covered the full development lifecycle, including requirements analysis, system design, implementation and piloting of modules at key customer sites.
A central theme throughout my work was the integration of third-party systems into the clinical platform.
Responsibilities
  1. Requirements analysis and design of clinical software modules
  2. Development of C#/.NET applications within the MCC.NET platform
  3. Design and implementation of interfaces to external clinical systems
  4. Technical coordination with integration partners (RIS, archiving and dictation systems)
  5. Maintenance of technical partnerships with third-party vendors to ensure stable integrations
  6. Database development with Oracle and MS SQL Server
  7. Pilot deployment of modules at customer sites and support of early production use
  8. Support of module rollout and pilot installations at key customers

Zertifikate

Build AI Agents using MCP

Coursera

2026

PSM I (Professional Scrum Master)

scrum.org

2026

IREB Foundation

Certible

2026

PRINCE2 Agile Foundation

PeopleCert

2026

Qdrant Essentials

Qdrant

2026

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