
Good Manufacturing Practice Experts in Essen
matched in minutes with AI and ready to support compliant productionHire experts who design GMP systems, prepare audit-ready documentation and improve quality processes across pharmaceutical, biotech, food and medical device operations. FRATCH connects you with vetted, available freelancers through fast, precise AI matching.
Meet FRATCH Experts in Essen, who have recently used Good Manufacturing Practice
Daniel J.
Last position:
Information Security Consultant
NIS2 Implementation Project and ISMS Development Based on IT-Grundschutz
Municipal utilities, public-law institution
- Analysis of the current compliance status regarding the requirements of the NIS Directive (NIS-2, EU 2022/2555).
- Identification of critical infrastructures and processes within the organization.
- Development of an action plan to meet NIS requirements.
- Conducting a risk analysis in accordance with BSI Standard 200-3 as the basis for the security concept.
- Preparation of an individual security concept including technical and organizational measures according to BSI IT-Grundschutz.
- Preparatory support for an optional certification according to BSI IT-Grundschutz.
- Adaptation of existing security policies and development of new ones for access controls, incident management and data protection.
- Consideration of municipality-specific requirements and integration of the measures into the existing IT infrastructure.
- Documentation of the results and preparation of audit-ready evidence for audits.
Tools, languages and frameworks used: MS Office, Verinice, IT-Grundschutz (200-x), NIS-2 (EU 2022/2555), ISMS, AI-Act (EU 2024/1989)
Alexander D.
Last position:
Interim Manager Procurement | Head of Procurement & Strategic Sourcing at Löwenstein Medical Technology GmbH & Co. KG
- Overall responsibility for strategic and operational procurement, Procurement Management (11 FTE).
- Further development of the procurement and procurement organization, including task and role model.
- Management of cross-functional special projects (e.g. value engineering, design-to-cost).
- Development and implementation of a holistic sourcing and procurement strategy with a focus on resilience, ESG, de-risking, decoupling and cost performance.
- Execution of a comprehensive procurement transformation with a new supply chain strategy alignment.
- Reorganization of the procurement team to improve efficiency through clear role allocation and relief from non-core and non-functional tasks.
- Professionalization of contract management processes and supplier development programs.
- Process optimization along the S2C and P2P chain, including standardization and automation in line with MDR (EU Regulation 2017/745), GxP compliance & quality management systems ISO 9001 and ISO 13485.
- KPI development and optimization of the KPI system for performance and efficiency measurement in critical paths and missing parts.
- Coaching the team in strategic procurement work, project management and procurement due diligence.
- Implementation of AI-supported tools for sourcing, spend analysis and inventory management to optimize inventory.
- Achieved inventory reduction of ~31% through professional inventory management.
- Management of two cost reduction (cost avoidance) programs with quantified results: ~50% reduction in manufacturing costs for one core component and ~64% reduction in material costs for the successor platform through redesign and category sourcing.
- Savings in the low double-digit million range versus the baseline.
- Material groups: contract manufacturing, PCBA, EMS, blower, silicone injection molding, power supplies, batteries, displays, hoses, masks, valves, foams, cables, sensors, wireless modules (2G–5G), telemedicine components, laboratory services.
Daniel U.
Last position:
Senior Application Packaging & Deployment Engineer at Allevio AG (Client: Allianz Technology)
- Enterprise application packaging and deployment for Allianz's global Windows migration programs across Europe, North America, and APAC
- Migrated hundreds of enterprise applications from Windows 10 VDI to Microsoft Azure Windows 365 (Windows 11)
- Created software packages in MSI/MST, FlexApp, PSADT 3/4, and App-V according to enterprise packaging standards
- Developed an ASP.NET packaging automation platform with MongoDB, SQL Server, SharePoint, and Outlook integration
- Built PowerShell modules for automated quality checks of MSI and FlexApp packages
- Developed a release conflict detection module in PowerShell to identify potential deployment issues before production
- Created WDAC monitoring scripts for automated policy oversight and incident response
- Implemented MSGraph API calls in PowerShell for Azure AD and Intune operations
- Created Citrix oData scripts for historical usage analysis (BYOD, VDI, fat clients)
- Developed an Intune Win32 app 'Do Not Disturb' deployment routine for an optimal user experience
- First point of contact for troubleshooting production incidents with packaged applications
- Coordinated application owner, UAT, and release testing for hundreds of deployments
- Administered Microsoft Intune, Citrix environments, and SQL Server security
- Created and tested WDAC policies in Intune; managed configuration policies and Win32 app deployments
- Primary packaging resource for Allianz France since 2019
Benjamin K.
Last position:
MDR Transition with PRRC-Function
- PRRC according to Article 15 MDR 2017/745
- Lead MDR transition for legacy products
- Communication with the notified body DQS
- Lead technical documentation
- Strategy in activities under MDR 2017/745
- Topics from the development department
- Risk management according to ISO 14971:2019
- Compliance and regulatory consulting for management/board
Mustafa K.
Last position:
Consultant (MBR Designer) at Bayer AG
Introduction of an MES system in pharmaceutical production.
Support in replacing existing recipes by introducing an MES system.
Focus on converting cleaning and manufacturing AKBs into MBRs.
System environment: Werum PAS-X MES, GMP, SAP, Microsoft Office (Word, Excel), XML
Pranav P.
Last position:
Executive – Quality Control Microbiology at Recipharm Pharma Services Pvt. Ltd.
- Performed microbiological analysis on pharmaceutical products ensuring compliance with industry standards
- Conducted MLT, BET, and environmental monitoring to maintain product quality
- Prepared method validation raw data and executed suitability testing
- Calibrated and maintained lab instruments including TOC analyzer, pH meter, incubators
- Collaborated with cross-functional teams to optimize testing workflows and reduce errors
Discover over 15,000 top freelancers
Statistics of experts using Good Manufacturing Practice
Aggregated from the professional profiles of matched freelancers.
Experience
22 years (Germany: 23 years)

Position duration
2.7 years (Germany: 3.1 years)

Positions per freelancer
18 (Germany: 13)

Top business areas
Quality Assurance, Operations, Information Technology

Top industries
Manufacturing, Pharmaceutical, Energy

Certification focus areas
Quality Assurance, Information Technology, Operations
Bachelor's degree or higher
60% (Germany: 92%)
Master's degree or higher
20% (Germany: 59%)

Certifications per freelancer
5 (Germany: 4)

Most common languages
German, English, French

Speak two or more languages
100% (Germany: 99%)
Based on our profile pool as of 29 Oct 2026.
Daily rate distribution
The chart shows how the daily rates of experts in this technology in Essen are distributed, based on recent contracts on our platform. Each bar covers a rate range — its height shows the share of experts charging within that range.
Average rates of experts in Essen using Good Manufacturing Practice
Rates are based on recent contracts and do not include FRATCH margin.
The average daily rate is the mean of all daily rates from recent contracts of comparable freelancers on our platform.
The median daily rate is the middle value of all daily rates — half of comparable freelancers charge less, half charge more. Unlike the average, it is barely affected by outliers.
Calculated based on our freelancers’ daily rates as of 29 Oct 2026. Actual rates may vary depending on seniority level, experience, skill specialization, project complexity, and engagement length.
Good Manufacturing Practice experts industry focus
See which industries our matched freelancers work in most often — every figure is calculated live from the freelancers on FRATCH.
- Manufacturing (83%)
- Pharmaceutical (67%)
- Energy (50%)
- Healthcare (50%)
- Transportation (50%)
- Retail (50%)
- Telecommunication (50%)
- Banking and Finance (33%)
Please note that freelancers can work across multiple industries, so percentages overlap.
About the technology
GMP foundations
Good Manufacturing Practice, commonly called GMP, is the framework for making products consistently and safely. It controls materials, facilities, equipment, personnel, records and release decisions across regulated production. The principles apply widely in pharmaceuticals, biotechnology, medical devices, cosmetics and selected food operations.
Quality systems
GMP work turns regulatory expectations into practical quality systems. Specialists define standard operating procedures, deviation and change-control workflows, CAPA processes, training records, supplier controls and batch documentation. They also connect quality assurance with production, laboratory, engineering and regulatory teams.
Tools and records
Professionals work with electronic quality management systems, document control tools, laboratory systems, manufacturing execution systems and validated spreadsheets. Their work may include:
- Creating and reviewing SOPs, master batch records and validation plans
- Managing deviations, investigations, CAPA and change control
- Preparing audit evidence, quality risk assessments and inspection responses
- Supporting data integrity, electronic signatures and controlled access
When companies need support
Companies often bring in freelance GMP expertise during facility start-up, product transfer, remediation or a quality-system upgrade. Specialists can provide focused support when an internal team faces an audit, a backlog of investigations, new market requirements or a transition to electronic records. In Essen and the surrounding Rhine-Ruhr region, collaboration may combine remote documentation work with on-site production or laboratory visits.
What strong experts deliver
Strong professionals understand both the written rule and the process behind it. They trace decisions to evidence, write clear documents, ask precise questions and distinguish a true compliance risk from unnecessary administration. They can communicate with operators, scientists, suppliers and leadership without losing technical accuracy.
- Risk-based, proportionate quality controls
- Inspection-ready records with clear ownership
- Practical training that teams can apply
- Independent review of systems, suppliers and processes
Selecting the right specialist
Look for experience that matches the product, process and regulatory setting rather than a generic GMP background. Discuss the scope of work, expected deliverables, site access, documentation standards and collaboration language before starting. A capable freelancer should explain how they will assess the current state, protect confidential data and leave the team with maintainable processes.
Frequently asked questions
The facts hiring teams ask for most often when it comes to Good Manufacturing Practice.
Good Manufacturing Practice is used to control how regulated products are made, tested, stored and released. It helps companies prevent contamination, mix-ups, errors and unreliable records while keeping processes consistent and traceable.
Good Manufacturing Practice focuses on product quality, patient or consumer safety and controlled production in regulated settings. ISO 9001 provides a broader quality-management structure, while GMP adds detailed expectations for operations, records, validation, investigations and release decisions.
A strong GMP specialist may also bring validation, quality risk management, data integrity, audit preparation and regulatory documentation skills. Knowledge of manufacturing, laboratory operations, supplier qualification or electronic quality systems is valuable when the assignment crosses team boundaries.
The right depth depends on the risk, product lifecycle and condition of the quality system. A document review may need a focused specialist, while remediation, inspection preparation or facility start-up calls for a professional who has led comparable work and can make sound decisions independently.
Good Manufacturing Practice assignments often combine remote work on procedures, records and investigations with on-site observations. Remote collaboration can work well when access, secure document exchange and clear communication are arranged; production-floor assessments and training may still require visits in Essen or nearby sites.
Many specialists can work in English, while German may be important for site procedures, operator training and local documentation. Confirm the required language for records, meetings and inspections before the assignment begins.
Ask the professional to explain their reasoning, evidence trail and approach to risk. High-quality GMP work produces clear ownership, consistent records, justified decisions and procedures that teams can follow in daily operations.
A Good Manufacturing Practice freelancer may deliver SOPs, gap assessments, validation documentation, audit responses, CAPA plans, training materials and quality-system improvements. The exact scope should be agreed with acceptance criteria, document owners and a process for handing work back to the internal team.
The average hourly rate of freelancers in Essen, Germany who have used Good Manufacturing Practice in their recent projects is 105 €, which corresponds to a daily rate of about 842 € based on an 8-hour working day.
Of the freelancers in Essen, Germany who have used Good Manufacturing Practice in their recent projects, 60% hold at least a Bachelor's degree and 20% hold at least a Master's degree.
On average, freelancers in Essen, Germany who have used Good Manufacturing Practice in their recent projects have 22 years of professional experience, with a single engagement typically lasting around 2.7 years.
The most common languages among freelancers in Essen, Germany who have used Good Manufacturing Practice in their recent projects are German (100%), English (100%), and French (17%).
The most common industries among freelancers in Essen, Germany who have used Good Manufacturing Practice in their recent projects are Manufacturing (83%), Pharmaceutical (67%), and Energy (50%).
The most common business areas among freelancers in Essen, Germany who have used Good Manufacturing Practice in their recent projects are Quality Assurance (100%), Operations (83%), and Information Technology (67%).
Main locations of FRATCH Experts, who have recently used Good Manufacturing Practice
Our freelancers and interim experts are at home across the DACH region — available on-site in the major business hubs or fully remote. Choose a location to discover matched specialists, local market insights and up-to-date availability.
Countries:
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