5s-Optimization in Offices & QC Laboratories - Online Training Recording

Course No. 21861



Dr. Karl-Heinz Bauer

Dr. Karl-Heinz Bauer

Boehringer Ingelheim International


The aim of this Live Online Training is to learn the basics of the 5s method and its five standardized steps. With the help of many practical examples from pharmaceutical laboratories and offices and numerous images, we will introduce you to this Lean method. We will also provide you with the tools to successfully introduce 5s in your company.


5s helps you take a systematic approach to improving workplaces and areas. The focus is mainly on order, cleanliness and standardization of offices & workshops.

The philosophy behind 5s is that cleaning-up is also checking, inspecting, or verifying. This method was developed by the Japanese car manufacturer Toyota and, along with many other tools, 5s is a central component of the Toyota production system. Even with little effort and cost, deviations can be discovered, and errors can be prevented more easily. 5s can be applied not only to laboratory or office/administrative areas, but also to all areas of pharmaceutical production (e.g. warehouse, manufacturing, packaging, workshops, service areas).

5s is an indispensable basic building block of lean management. In a joint study by the Fraunhofer Institute for Production Engineering and Automation (IPA) and the Kaizen Institute Germany, a significant improvement potential of up to 30% was found in the administrative areas of companies, which can even be exceeded in laboratory areas.

After the introduction of 5s, audits and a process for continuous improvement (CIP) will serve you to maintain and further improve the achieved conditions in terms of order and cleanliness, with the aim of:
  • Organization of the workplace
  • Increasing occupational safety
  • Reduction in idle and search times
  • Increase efficiency
  • Increase of productivity
  • Improving workplace appearance & structure

Target Group

This Live Online Training is aimed at employees and managers in the pharmaceutical industry, especially in the following areas:
  • ƒPharmaceutical quality control
  • Pharmaceutical development
  • Quality assurance
  • Contract laboratories
  • Service providers
Also addressed are all employees and managers who work in an administrative work environment (offices, warehouses, archives, etc.) as well as employees who share a workstation in the office with others.

Technical Details

To participate in an on demand training course or webinar, you do not need any software. The recordings are made available via a streaming server. In general, the recording is provided in MP4 format, which any PC (Microsoft Windows, Apple IOS) or tablet can easily display.

Timing and Duration:
When you register for the on demand Training course or webinar you can decide at what date you want to follow the training course online. For a 1-day training course you will have 2 days in which the stream is available (for 2-day training course 3 days and for a 3-day training course 4 days). Within in this timeframe you can start & stop the stream according to your needs.

In time before the scheduled date (your desired date) you will receive an e-mail from us with a link for direct participation as well as your log-in data.

Please be aware: The recording does not include the Q & A sessions.

Training Course Documentation and Certificate:
The presentation will be made available as PDF-files via download during the online training course. After the successful completion of the online training, you are able to download the certificate of attendance.


Welcome and Introduction

Learning about Kaizen and the 5s Tools
  • Introduction and overview of 5s
  • Terms and definitions
  • Relation to Lean Management and Kaizen
  • The 7 types of waste
  • The origin of the 5s method
  • 5s as a basic building block of lean Management
  • Goals & benefits of 5s
  • 5s in Detail
  • Practical examples of 5s in office and administrative areas
Practical Exercise on 5s: „The Number Game”
The exercise consists of 6 phases, which represent the 5 steps of optimization:
  • Sort
  • Set in order (systematize)
  • Shine (clean up)
  • Standardize
  • Sustain (improve systematically)
goes through step by step and makes the process improvement clearly measurable and understandable for the participant.

Detailed 5s Standardization and Use Cases in QC Laboratories
  • Transferability from 5s in the office to 5s in the lab
  • Advantages of 5s in the lab
  • Practical examples of 5s in the laboratory
  • Practical examples of checkpoint-related workstations in the laboratory
  • Practical examples in everyday laboratory work for the supply and disposal of QC labs with
    - Glassware,
    - Disposables & auxiliary materials and
    - Chemicals
    - As well as the disposal of waste.
Tools to assure Sustainability of 5s in Laboratories and Offices
  • 5s-Audits
  • CIP (Continuous Improvement Process)
  • 5s-Trainings & -Instructions
  • 5s-Walkabouts
  • Performance indicators
  • Visualization of 5s and 5s-improvements
Recording from 19.06.2024
Duration of the recording: approx. 3 h 15 min.

ECA-Member*: € 590,-
Regular Fee*: € 690,-
EU/GMP Inspectorates*: € 590,-
APIC Member Discount*: € 640,-

(All prices excl. VAT). Important notes on sales tax.

* also payable by credit card
American Express Visa Mastercard

Further dates on-site
Further dates on-site
Not available
Further dates online
Further dates online
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Do you have any questions?

Please contact us:
Tel.: +49 6221 8444-0
E-Mail: info@gmp-compliance.org

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