Good Laboratory Practice Experts in Germany
matched in minutes from over 15,000 CVs with vetted, available specialists.Hire experts who support GLP inspection readiness, study records, SOP alignment, and audit preparation across regulated labs. They help with OECD GLP, documentation control, and quality systems, with fast, precise matching to vetted, available freelancers.
Meet FRATCH Experts in Germany, who have recently used Good Laboratory Practice
Jozsef Ferincz
Last position:
IT project management, introduction of AI-supported software development
- Industry: software manufacturer
- Tasks: project management; tracking and coordination of projects; stakeholder management; change management; prioritization of requirements; alignment of architecture; supplier management (internal and external); release management; monitoring defect resolution with the teams; AI-supported software development, software testing and code analysis; AI prompting, prompt engineering
- Software: Jira, Confluence, MS Project, MS Teams
- Environment: IT, software development, agile, artificial intelligence (AI)
Alex Volnov
Last position:
CTO, Co-Founder, Cryptography(incl. Post-Quantum Cryptography) and AI Security Expertise at AISLEIPNIR
- Integration of Post-Quantum Cryptography (PQC) algorithms into high level protocols.
- Security of implementations of Post-Quantum Cryptography algorithms.
- Transition to Post-Quantum public key infrastructures.
- Security evaluations of Post-Quantum Cryptography (PQC) primitives.
- Drone Cybersecurity
- Satellite Cybersecurity
- AI Security
Ricarda Mayer
Last position:
Consultant Quality Management at Quality for Life Sciences (Consulting)
- Quality assurance / management
- Process optimization (laboratory processes, QM/QS processes, etc.)
- Revision and adaptation of existing systems (e.g. document management, equipment management) to ensure compliance with new regulatory requirements
- Implementation/optimization of deviation and/or change control management processes
- GLP and GMP support
- Interim Quality Manager
- QA management
- Audits and inspections
- Conducting internal audits / self-inspections (GLP, GMP)
- Organization, preparation, coordination and support of regulatory inspections including creation of action plans if needed
- Creation and revision of controlled documents (SOPs, qualification documents, manufacturing instructions, checklists, forms, etc.)
- Content review of existing controlled documents for compliance, structure/format and consistency
- "Streamlining" of document management systems
- Basic training (GLP, GMP)
- Refresher training (GLP, GMP)
- Equipment qualifications
- Other topics on request
Adrien Junior Mbialeu Ii
Last position:
Sample Manager Bioanalysis at Abbvie Deutschland
- Quality assurance and management of bioanalytical study data in LIMS and ELN systems
- Ensuring compliance with GLP and GCP in clinical studies
- Supporting project teams on quality and compliance issues
- Quality control and adherence to regulatory requirements
- Assessing data integrity, traceability, and study processes
- Close collaboration with QA, lab, and study teams in a pharmaceutical environment
- Qualification and validation of various equipment (e.g., air samplers, data loggers, freezers, refrigerators, incubators)
- Maintenance and calibration of various equipment (e.g., air samplers, data loggers, sensors)
- Deviation management
- Qualification and maintenance of monitoring systems (pressure, temperature, room temperature and humidity sensors) including alarm systems
- Executing qualification and validation activities: CC, CQ, IQ, OQ, PQ, RA, CR, CAPA, DQ
- Creating and reviewing URS, RTM, test plans, and qualification documentation
- Reviewing, maintaining, and tracking quality-related documentation
Sejalkumari Patel
Last position:
Regulatory Documentation Specialist at VRS Healthcare
- Prepared and reviewed finished product and raw material specifications as per USP, BP, EP, IP, and in-house standards.
- Developed and reviewed SOPs, analytical method validation and transfer, and comparative dissolution studies.
- Reviewed stability, DMF, and cleaning validation documents; resolved regulatory queries.
- Supported QA and RA departments to ensure compliance with GMP and site audit readiness.
Monika Weber
Last position:
Quality Specialist at Nexans GmbH
- Implementation of a quality management system including creating all required process descriptions and work instructions for ISO 9001:2015 certification, as well as final planning and conducting audits
- Creating action catalogs for measures needed to comply with ISO 9001 and achieve the targeted certification
- Preparing documentation related to ISO 9001
- Developing training materials for employees and managers based on the QMH and the created documentation
- Recording results of external audits of departments (incoming goods, production, warehouse logistics, procurement and supplier management, outgoing goods, shipping) according to ISO 9001
- Preparing for and participating in certification audits
Desalegne Syit
Last position:
Medical Device Auditor (ISO 13485, ISO 9001) at DQS Medizinprodukte GmbH
- Conducting external audits in medical technology with a focus on GMP, MDR and QMS compliance
- Assessing CAPA actions, validation documents and regulatory study materials
- Training teams in audit readiness and quality awareness
Petal Smart
Last position:
Senior Associate/Consultant, Quality Assurance at Elanco Animal Health
- Conducted GCP/GLP audits, compiled quality metrics, supported inspection and documentation for regulatory submissions
- Collaborated with clinical, technical, regulatory, study execution, and management teams
- Reviewed systems and processes in preparation for EU and global regulatory filings
- Edited quality and regulatory documents for internal and external review
Niels Adams
Last position:
Consultant: Translational Sciences at Large Pharma
- Authoring biomarker planning documents, biomarker manuals, research and development reports
- Review of clinical trial and vendors’ biomarker reports
- Development of standard operating procedures and interdepartmental training materials
Nandkishor Virani
Last position:
Bioinformatics Analyst at Dr. Omics Research Lab
- Analyzed large-scale genomic, transcriptomic, and proteomic datasets using bioinformatics tools and pipelines.
- Performed data preprocessing, quality control, alignment, and variant identification using platforms like Python, R, and Linux-based tools.
- Conducted statistical and computational analyses to identify biomarkers, gene expression patterns, and functional annotations.
- Collaborated with laboratory scientists to integrate bioinformatics results with experimental data.
Olaf Schneider
Last position:
Senior Supplier Quality Engineer for Sanitary Products at Grohe AG
- Responsible for carrying out sample approval processes
Amara El Madak
Last position:
Qualification Engineer at Optima Pharma GmbH
- Qualification of filling lines
- Preparation of IQ, OQ, PQ documents and reports
- Execution of FAT and SAT
- Alarm lists: create and perform tests
- Preparation of GMP-compliant documentation (qualification plan, URS, risk analysis, IQ, OQ, PQ and qualification report)
Pranav Padinjare Kanisantavita
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
Said Waezsada
Last position:
HSE Manager at Worley
- Consultation on HSE-related topics
- Preparation of relevant documents (EHS plans)
- Construction inspections
- Construction meetings
- Construction briefing
- Review of contractors' risk assessments
Kai Jeske
Last position:
Freelancer / QM Consultant at ValiQuali.de
- Qualification of production facilities and process validations of a new production line for the manufacture of implants incl. URS, IQ, OQ and PQ
- Quality remediation project (optimization of procedures, SOP and test methods and work instructions incl. change management)
- Project lead for a test method validation
- CAPA management
- Non-conformance management
- Gap analysis
Discover over 15,000 top freelancers
Statistics of experts using Good Laboratory Practice
Aggregated from the professional profiles of matched freelancers.
Experience
22 years
Position duration
1.8 years
Positions per freelancer
13
Top business areas
Quality Assurance, Research and Development, Project Management
Top industries
Pharmaceutical, Healthcare, Biotechnology
Certification focus areas
Quality Assurance, Human Resources, Information Technology
Bachelor's degree or higher
93%
Master's degree or higher
73%
Doctorate
47%
Certifications per freelancer
3
Most common languages
German, English, French
Speak two or more languages
100%
Based on our profile pool as of 30 Aug 2026.
Daily rate distribution
The chart shows how the daily rates of freelancers in this technology in Germany are distributed, based on recent contracts on our platform. Each bar covers a rate range — its height shows how many freelancers charge within that range.
Average rates of experts in Germany using Good Laboratory 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 30 Aug 2026. Actual rates may vary depending on seniority level, experience, skill specialization, project complexity, and engagement length.
About the technology
GLP basics
Good Laboratory Practice, often called GLP or OECD GLP, defines how non-clinical laboratory studies are planned, run, recorded, and archived. It is used in safety testing, regulatory submissions, and studies that must stand up to inspection. Strong experts keep work traceable from protocol to final report.
Typical work
- Drafting or reviewing SOPs, protocols, and study plans
- Checking raw data, logbooks, and report consistency
- Preparing for internal audits and authority inspections
- Building document control and archive routines
- Closing gaps in data integrity and traceability
Where it matters
Companies bring in GLP specialists when a lab starts regulated work, expands its study portfolio, or needs to fix findings after an audit. In Germany, this often touches contract labs, chemicals, pharma, biotech, and testing teams that work with external regulators. Remote support works well for document review, while on-site work helps with process walks and inspection prep.
What good experts do
A strong specialist knows the difference between running experiments and running compliant studies. They understand roles, responsibilities, deviations, CAPA, training records, and archive handling. They also know how to make procedures practical so the lab can follow them without slowing the science.
Tooling and systems
GLP work is not one software stack, but experts often work with quality management systems, document control tools, LIMS, and audit tracking records. They should be comfortable reading controlled forms, version histories, and study master files. For teams in Germany, clear written communication in English is often essential; German helps on site.
When to hire
- You are setting up GLP processes for the first time
- An inspection found gaps in records or traceability
- Your study team needs support with OECD GLP expectations
- You must align multiple labs or external partners
- You need temporary coverage for quality or compliance work
Frequently asked questions
Need clarity? These are the questions we hear most often about Good Laboratory Practice.
Good Laboratory Practice is used to make non-clinical laboratory studies traceable, repeatable, and ready for regulatory review. It matters in safety studies, toxicology, analytical testing, and any work where records must clearly show what was done, when, and by whom. Companies use it to reduce compliance risk and keep study data defensible.
GLP is related to both, but it serves a different purpose. GLP focuses on the conduct and documentation of non-clinical studies, while GMP covers manufacturing and ISO 17025 focuses on testing and calibration competence. A strong expert should know where the boundaries sit and when one system overlaps with another.
A strong Good Laboratory Practice specialist usually brings SOP writing, audit preparation, deviation handling, CAPA support, and document control. Experience with study plans, raw data review, and archive management is important too. If the work touches regulated reporting, familiarity with quality systems and inspection language is a plus.
The right level depends on the gap you need to close. A small documentation review may only need a specialist with solid GLP process knowledge, while a full inspection response or system setup needs deeper hands-on experience with regulated studies. Look for proof of work in similar lab environments, not just general quality work.
GLP work can often be split between remote and on-site tasks. Remote support is good for SOP review, gap analysis, training materials, and report checks, while on-site time helps with lab walks, interviews, archive checks, and inspection preparation. In Germany, hybrid work is common when the lab and the expert agree on access and language needs.
OECD GLP is the most common reference point for internationally recognized non-clinical study quality. Many companies use the term Good Laboratory Practice in a broader sense, but the practical expectations usually come from OECD principles and national inspection practice. A good specialist should be able to work within that framework without overcomplicating it.
A strong Good Laboratory Practice freelancer gives clear examples of regulated studies, audits, and corrective actions they supported. They should explain how they improved traceability, fixed documentation issues, and helped teams stay inspection ready. Good signs are practical thinking, calm communication, and a clear grasp of what regulators look for.
GLP often sits next to QA, regulatory affairs, data integrity, and laboratory operations. In many projects, the same specialist also helps with SOP governance, training records, controlled documents, and inspection response writing. If your work spans multiple sites or external labs, coordination skills matter as much as technical GLP knowledge.
The average hourly rate of freelancers in Germany who have used Good Laboratory Practice in their recent projects is 87 €, which corresponds to a daily rate of about 693 € based on an 8-hour working day.
Of the freelancers in Germany who have used Good Laboratory Practice in their recent projects, 93% hold at least a Bachelor's degree, 73% hold at least a Master's degree, and 47% hold a doctorate.
On average, freelancers in Germany who have used Good Laboratory Practice in their recent projects have 22 years of professional experience, with a single engagement typically lasting around 1.8 years.
The most common languages among freelancers in Germany who have used Good Laboratory Practice in their recent projects are German (100%), English (100%), and French (20%).
The most common industries among freelancers in Germany who have used Good Laboratory Practice in their recent projects are Pharmaceutical (80%), Healthcare (73%), and Biotechnology (60%).
The most common business areas among freelancers in Germany who have used Good Laboratory Practice in their recent projects are Quality Assurance (100%), Research and Development (73%), and Project Management (60%).
Main locations of FRATCH Experts, who have recently used Good Laboratory 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.
Berlin Hamburg Munich Cologne Frankfurt Stuttgart Dusseldorf Leipzig Dortmund Essen Bremen Dresden Hanover Nuremberg Request a free demo
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Philipp Thomaschewski
FRATCH CEO
