Skip to main content Skip to search Skip to main navigation

Human Resource Management as a Key to Success

Excerpt from the GMP Compliance Adviser, Chapter 2.A, Human resource management

4 min. reading time | by Michael Hiob, PhD
Published in LOGFILE 03/2026 

Qualified personnel contribute significantly to the long-term success of a company and thus to its long-term security. Against the backdrop of demographic change and the increasing shortage of skilled workers, effective human resource management is becoming increasingly important for ensuring the competitiveness of a company. Learn more about goals, tasks and methods in chapter 2.A Human resource management in your GMP Compliance Adviser.


Employees are more than just production and cost factors!

The pharmaceutical industry in Germany and other countries, too, faces considerable challenges in the area of human resource management. These problems have far-reaching implications for the competitiveness and innovative power of the industry. The shortage of skilled workers has become significantly more acute in the pharmaceutical industry in recent years. Demographic change is forcing all industries to compete for available skilled workers. There is a shortage of university placements and training opportunities for pharmacists. These bottlenecks not only hinder the further development of the industry but also jeopardize the supply of important medicines. To overcome these challenges, pharmaceutical companies must develop innovative strategies for recruiting and retaining personnel, invest in training and continuing education, and possibly also explore new approaches to how work is organized. In addition, close cooperation between industry, educational institutions, and policymakers is necessary to improve the framework conditions for skilled worker development in the pharmaceutical industry.

Against this backdrop, effective human resource management that takes into account both the economic goals of the company and the personal interests of its employees is of crucial importance. Companies that successfully avoid conflicts of interest in this area will be successful in the long term. Conversely, poor human resource management jeopardizes the success of the company and the motivation of its employees. It is their motivation that determines whether new improvement ideas are proposed, working time is used as efficiently as possible, and resources are used economically. The source of this motivation to work is not solely a question of performance-related pay. In many cases, the general conditions at the workplace (e.g. corporate culture, work atmosphere, flexible working hours, quality of the canteen) determine whether someone identifies with their company. Personnel in pharmaceutical companies must be regarded as part of the company's intangible assets. They contribute significantly to the long-term success of the company and thus to its long-term security. 

Tasks of senior management 

Senior management plays a key role in shaping human resource management. In order to achieve the goals of the quality policy, senior management must define a personnel policy and a personnel strategy derived from it. In addition, senior management are obliged to provide adequate human resources to achieve quality objectives. Through their role model function, strategic orientation, and active shaping, they also exert a decisive influence on the corporate culture. Senior management also plays a decisive role in the successful implementation of organizational development. Last but not least, senior management are obliged to conduct regular reviews of human resource management. 

What are the core tasks of human resource management? 

The core tasks of human resource management are diverse and include all activities and strategies that deal with a company's employees. These include personnel planning and marketing, staffing and recruiting, human resource development and management, as well as human resource administration and compensation management. Human resource management thus covers the entire life cycle from hiring to leaving the company. 

What are the basic requirements for organizational structures? 

A clear organizational structure that corresponds to the tasks and goals of the company is an essential basis for effective human resource management. Good structure, efficient communication, and the avoidance of overlap promote the effectiveness and efficiency of departments and thus make a significant contribution to the success of the company. In a dynamic environment, specialization, flexibility, and adaptability are becoming increasingly important. 

Which different forms can be chosen for the organizational structure? 

When designing the organizational structure, a fundamental distinction must be made between stability-oriented and change-oriented organizational structures. When selecting a company-specific structure, it is important to find the right balance between stability and flexibility. It is crucial that the chosen structure optimally supports the company's goals. 

How do you design departments, positions, and workplaces? 

Departments are an essential element of the hierarchical corporate structure. They are typically represented in organisational charts to illustrate the organisational structure graphically. Each department represents a distinct area to which specific tasks, responsibilities, and employees are assigned. 

The smallest organisational unit in a company is called a job or position, depending on the level of responsibility. In line organisations, a distinction is made between management positions, executive positions, and support positions. The specific tasks of employees in positions of responsibility must be set out in job descriptions.


Do you have any questions or suggestions? Please contact us at: redaktion@gmp-verlag.de


Dr. Michael Hiob
Dr. Michael Hiob

You may also be interested in the following articles:

Outsourced Activities in the GDP Environment Part II: Contractual Agreements

Outsourced Activities in the GDP Environment Part II: Contractual Agreements

When outsourcing GDP activities, there is a need for concrete delimitation of responsibilities between a client and a contractor. Read more about the goals and the contents of a quality agreement in the following excerpt from GMP:KnowHow Pharmalogistics (GDP).

Read more
Question of the Week | GMP-Verlag

What are the Benefits and Limitations of Passive Temperature-Controlled Containers for Drug Transport?

Here's the answer:
Read more
FDA: Adjustment of Nitrosamine Limits for Short-Term Use Medicines

FDA: Adjustment of Nitrosamine Limits for Short-Term Use Medicines

The FDA has updated its recommendations on Acceptable Intake (AI) limits for nitrosamine impurities. Under certain conditions, the Agency now accepts a Less-Than-Lifetime (LTL) adjustment of AI limits for medicinal products that are not intended for lifetime use. This also represents an alignment with the LTL concept of ICH M7(R2).
Read more
Swissmedic: SMS Registration Becomes Prerequisite for GMP Certificates

Swissmedic: SMS Registration Becomes Prerequisite for GMP Certificates

As of 15 November 2026, active substances must be registered in the EMA's Substance Management Services (SMS) database before Swissmedic can include them in establishment licences and GMP certificates for active substance manufacturers. The new requirement results from modifications to the EudraGMDP database.
Read more
News: EMA

EMA: New Q&As for Biological Medicinal Products

The EMA has added a new section to its Q&As on biological medicinal products addressing medicinal products containing secretomes or extracellular vesicles (EVs) obtained from human or animal cells.
Read more
News: Europe

EU: Council Adopts the Pharmaceutical Package

On 28 September 2026, the Council of the European Union adopted the EU pharmaceutical package, marking another important step in the legislative process for the comprehensive reform of EU pharmaceutical legislation.
Read more
Previous
Next

Related Products

Skip product gallery
GMP Compliance Adviser | Named User Licence | 12M

GMP Compliance Adviser | Named User Licence | 12M

With an named user licence, one user can access the knowledge portal; with a corporate licence, any number of users can access it.Approx. 5,000 pages of practical GMP knowledge with illustrations and forms: Practical guidance for rapid implementation in the workplaceDetailed descriptions of GMP-compliant systemsInternational laws and guidelines Always up-to-date thanks to regular updates Download Advantages and Prices60+ Sample Documents In addition, the GMP Compliance Adviser contains more than 60 sample documents (MS Office) and practical examples that you can use.Sample SOPsSample FormsSample ReportsSample DocumentationChecklistsProcess Diagrams (Flowcharts)Practical Examples of QRM Application (e.g., Risk Analyses)Sample Documents for Qualification and ValidationCase StudiesWritten by more than 80 authors with hands-on experience directly linked to the industryA team of over 80 experts interpret regulatory requirements and describe how they are implemented in practice.The authors are experienced in the pharmaceutical industry, consulting, and government agencies.

delivery immediately after receipt of payment
€1,368.00 net excl. VAT
GMP:KnowHow Pharma Logistics (GDP) | Named User Licence | 12M

GMP:KnowHow Pharma Logistics (GDP) | Named User Licence | 12M

Your knowledge portal for GDP-compliant pharmaceutical logistics.  It is important that you as a logistics service provider, but also as a client in the pharmaceutical industry, comply with regulatory requirements. The GMP:KnowHow knowledge portal guides you through the complex regulatory landscape of the pharmaceutical and logistical supply chain! The knowledge portal gives you an easy-to-understand overview of all the important topics. Interactive graphics help you navigate all areas covered by the EU GDP Guidelines (2013/C 343/01). You also have the relevant passages of the regulations directly at hand for each topic. This allows you to compare the requirements directly and saves valuable research time.One thing is certain: the knowledge portal answers your questions about the supply chain of medicinal products, active pharmaceutical ingredients and medical devices. You don't have to be an expert. Yet.You will find answers to your questions in the GMP:KnowHow Pharma Logistics (GDP). Where does GDP begin, where does GMP end? What does GDP-compliant mean? When do I also have to take GMP requirements into account? What permits do I need for certain activities? What requirements do I have to fulfil? What is the current legal basis? How am I covered? What authorizations do I have for my work, e.g. from my employer? Who is responsible — the client or the contractor? And many more What is the difference to the GMP Compliance Adviser? GMP:KnowHow Pharma Logistics (GDP) is a practical knowledge portal dedicated to Good Distribution Practice (GDP). It is a product that is independent of the GMP Compliance Adviser and concentrates on content that is essential for carriers of medicinal products, active pharmaceutical ingredients and medical devices as well as for logistics clients. The focus is on practical knowledge and how to apply it in your daily business. If necessary, the relevant regulations can be called up immediately alongside the practical knowledge, and you can see the relevant paragraphs at a glance. In addition, sample documents are available to help you make immediate progress. AuthorSimone Ferrante, currently Director Quality at Fisher Clinical Services, previously served as Head of Quality Control and Responsible Person (GDP) for the Grieshaber Group. She is also a long-standing author and GDP expert at GMP-Verlag.

delivery immediately after receipt of payment
€610.00 net excl. VAT
E-Learning GMP:READY | Specialist Knowledge GMP for Engineers

E-Learning GMP:READY | Specialist Knowledge GMP for Engineers

Why are GMP rules important for technicians and engineers? Technicians and engineers play a key role in ensuring compliance with Good Manufacturing Practice (GMP) standards. They are involved in critical activities such as: planning and construction of ventilation systems, maintenance of water treatment plants, calibration of measuring sensors. Therefore, they are jointly responsible for the quality of medicines and must ensure that their work complies with GMP standards.Your advantages: Fast familiarization with GMP topics in approx. 2 hours, time- and location-independent online training, printable personal certificate, 12-month access for initial and follow-up training, automatic updates in case of legal changes,content compliant with Article 7(4) of Directive 2003/94/EC.The Author This e-learning course was developed with the collaboration of Dipl.-Ing. Andreas Nuhn (D & B Pharmadesign GmbH).

delivery time appr. 2-5 workdays after receipt of payment
€245.00 net excl. VAT
GMP Fundamentals | A Step-by-Step Guide

GMP Fundamentals | A Step-by-Step Guide

This handbook is a practical and easy to read guideline, giving you a quick and comprehensive overview of the complex world of Good Manufacturing Practice (GMP) without the need of previously acquired knowledge. Some topics are: GMP: Purpose and basic pharmaceutical terms Laws, licenses and inspections Personnel: Responsibility and hygiene Standard Operating Procedures (SOP) and documentation Design of rooms and facilities Processing and packaging Quality control and market release Suppliers, storage and logistics (Good Distribution Practice = GDP) Alphabetical index and abbreviations Using practical examples and comparisons to every-day life will help to easy understand GMP regulations.GMP Fundamentals is a helpful guide which facilitates the entry into the GMP world and teaches the necessary basics.

delivery immediately after receipt of payment
€44.90 net excl. VAT