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Good Manufacturing Practice Experts in Frankfurt

in minutes from vetted and available specialists

Hire experts who design GMP-compliant processes, prepare audit-ready documentation, and support validation, quality systems, and clean-room operations. Fast, precise matching with vetted, available freelancers.

Meet FRATCH Experts in Frankfurt, who have recently used Good Manufacturing Practice

Verified expert

Achim Klein

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Portfolio Manager, Consultant, Leadership Coach

Hofheim am Taunus
Achim Klein

Last position:

Portfolio Manager, Consultant, Leadership Coach at Abbvie Deutschland GmbH &Co. KG

  • Management and optimization of a portfolio of about 100 projects (launches, in-field solutions, data & analytics, digital solutions, digital products)
  • Optimization of the existing project standard (playbook) and alignment with the European and global organization (USA)
  • Coaching project managers on setup, planning, cooperation with business, GDPR, GxP, data security and launches
  • Preparing projects for works council information and project closeout communication
  • Optimization of resource management (tracking, allocation, prioritization)
  • Taking over individual project leads (off-/transboarding, event management, checking whether WhatsApp is allowed on a business smartphone)
  • Supporting the hiring of external project managers
  • Optimization of meeting structure, project controlling (KPIs), change and demand management
  • Optimization of risk, issue, dependency and quality management and support during internal audits (GxP)
  • Optimization of the portfolio steering tool (Smartsheet) on national, European and global level
  • Design and implementation of a Business Value Complexity Scoring
  • Building a strategic PMO with a sister department and optimizing cross-functional teams
  • Reporting, communication and escalation at management level
  • Leadership coaching for several future leaders (short-time assignment)
  • Development of the concepts "PPM as a Service" and "Internal Customer Approach"
  • Development and review of a concept "AI Data Governance" including roles and processes
  • Selection and onboarding of the successor
Verified expert

Adrien Junior Mbialeu Ii

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Sample Manager Bioanalysis

Langen (Hessen)
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
Verified expert

Isaac Udoh

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Global Head of Quality, Safety and Regulatory Affairs

Schmitten im Taunus
Isaac Udoh

Last position:

Global Head of Quality, Safety and Regulatory Affairs at RKW SE

  • Development and implementation of global quality, safety and regulatory affairs strategies.

  • Transformations in quality, safety, and regulatory affairs.

  • Lead RKW to deliver the quality promised to the customers and grow the business.

  • Lead RKW to successfully achieve the zero-safety incident journey.

  • Lead RKW to successfully achieve regulatory affairs compliance journey.

  • Envisioned, designed, and implemented a global quality, safety and regulatory affairs strategy for the RKW global business.

  • Successfully involved all 14 RKW sites in global quality and safety plan as lead site and/or roll out site.

  • Introduced safety, quality, master plan and safety A3 to all 14 RKW sites contributing to double digits €-Million EBITDA Y2024.

  • Included quality and safety into the company bonus system.

  • Led global workshops to build Root Cause Problem Solving capability across entire company (209 persons trained) and Job Safety Analysis capability (100 persons trained).

  • Introduced globally the top 3 quality defects/losses elimination using RCPS tool contributing to double digits €-Million EBITDA Y2024.

  • Regained confidence of top customers (Procter & Gamble, Essity, Ontex) via solid implementation of global quality strategy.

  • Reduced cost of claims by 35% (Y2024 vs Y2023).

  • Established a solid safety foundation and standards enabling continuous improvements in incident rate globally.

Verified expert

Shreya Bhattacharya

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Technical Leader

Neu-Isenburg
Shreya Bhattacharya

Last position:

Technical Leader at SLK Software

  • Participate in quality workshops for requirements gathering and fit/gap analysis
  • Demonstrated different QMS modules/processes with focus on customer requirements
  • Design and implementation of cloud based quality system reducing manual efforts for the client
  • Collaboration with cross functional teams to define and document system requirements
  • Understanding the existing business process flow and suggesting improvements over moving to new quality systems
  • Managed the implementation of a data migration strategy from legacy system to cloud
  • Providing solution walkthrough to the business users
  • Involved in integration of quality system with different third party systems
  • Preparing weekly status report and presenting the same to business users and project stakeholders
Verified expert

Philipp Hofmann

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Director Pharmacovigilance, Global QPPV

Frankfurt am Main
Philipp Hofmann

Last position:

Director Pharmacovigilance, Global QPPV at Navitas Life Sciences

  • Management of the global Pharmacovigilance (PV) department
  • Manage post-authorization PV and safety in clinical trials (all phases)
  • EU-QPPV, National Safety Officer (Stepwise Action Plan Officer), Medical Information Officer
  • Management and reporting of Adverse Drug Reactions and Serious Adverse Events
  • Maintain and develop PV system
  • Medical project management (particularly multinational clinical trials)
  • Medical review of documents and data for projects
  • Support of preparing clinical research documents, e.g. study protocol, DSURs, PSURs, safety management plan, final report
  • Internal and external medical trainings
  • Active participation in business development for PV
Verified expert

Desalegne Syit

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Medical Device Auditor (ISO 13485, ISO 9001)

Schwalbach am Taunus
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
Verified expert

Amara El Madak

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Qualification Engineer

Flörsheim am Main
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)
Verified expert

Britta Schüle

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Project Leader

Kronberg im Taunus
Britta Schüle

Last position:

Project Leader

  • Development of NLP (AI) products for public administration, meeting increased security requirements
  • Administrative assistant with chatbot support for drafting emails and invitations
  • Intelligent search for parliamentary inquiries with keywords, text highlighting, and linking to additional information
  • Led a team to build prototypes to test product ideas in the NLP/AI area
  • Company-wide contact for NLP (AI) products
  • Established processes for in-house product development
  • Created and conducted quality gates
  • Supported an agile team as Scrum Master
  • Built scalable structures according to SAFe (Scrum of Scrums, Problem Solving Workshop, Single Source of Truth)
  • Formed and shaped the team (Kick-off, Pulse Checks, Retrospectives)
  • Moderated SoS, Kick-offs, regular meetings, and PL/SM workshops
  • Supported and coached an inexperienced Product Owner

Discover over 15,000 top freelancers

Statistics of experts using Good Manufacturing Practice

Aggregated from the professional profiles of matched freelancers.

Experience

20 years (Germany: 23 years)

Position duration

2.2 years (Germany: 3.2 years)

Positions per freelancer

12

Top business areas

Quality Assurance, Product Development, Project Management

Top industries

Pharmaceutical, Healthcare, Information Technology

Certification focus areas

Information Technology, Project Management, Quality Assurance

Bachelor's degree or higher

90% (Germany: 92%)

Master's degree or higher

50% (Germany: 58%)

Doctorate

10% (Germany: 18%)

Certifications per freelancer

3 (Germany: 4)

Most common languages

German, English, French

Speak two or more languages

100% (Germany: 99%)

Based on our profile pool as of 30 Aug 2026.

Daily rate distribution

0 1 2 3 4
<€480 €480-​640 €640-​800 €960-​1120 €1120-​1280 €1280+

The chart shows how the daily rates of freelancers in this technology in Frankfurt 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 Frankfurt using Good Manufacturing Practice

Rates are based on recent contracts and do not include FRATCH margin.

1000
750
500
250
Rate comparison chart
Daily rate avg. 888 €
Germany avg. 911 €

The average daily rate is the mean of all daily rates from recent contracts of comparable freelancers on our platform.

1000
750
500
250
Rate comparison chart
Median rate 980 €
Germany median 920 €

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

GMP basics

Good Manufacturing Practice sets the rules for producing safe, consistent, and traceable products. In practice, GMP work covers controlled procedures, documentation, training, deviations, and change control across regulated production sites. It is central in pharma, biotech, food, cosmetics, and medical device environments.

What experts deliver

A strong GMP specialist turns rules into daily routines that people can follow. Typical work includes:

  • SOP writing and review
  • batch record design and gap checks
  • deviation, CAPA, and change control support
  • audit preparation and follow-up
  • validation support for equipment, cleaning, and processes

Tooling and systems

GMP work often sits next to quality systems, document control, and production software. Specialists need to understand how data flows through eQMS, LIMS, MES, and training records, and how those tools support traceability. Strong professionals also know how to connect process design with practical shop-floor use.

When companies need help

Companies bring in freelance GMP expertise when a site is scaling, a new product is moving into production, or an audit is coming up. In Frankfurt, this is often relevant for organizations tied to pharma, life sciences, and advanced manufacturing. Interim support is also useful when internal quality teams need extra capacity for documentation or remediation.

What strong specialists do

The best professionals do more than quote the rules. They spot weak controls, close documentation gaps, and keep production moving without losing compliance. They communicate clearly with quality, operations, and engineering teams, and they know when to push for a stricter control or a simpler, workable process.

Work model and fit

Some GMP tasks are fully remote, such as document review, SOP updates, and audit preparation. Others need on-site presence, especially for line walks, training, inspections, or production support. In Frankfurt, companies often look for experts who can work in English and coordinate smoothly with local teams when German documentation or plant access is involved.

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Frequently asked questions

What clients ask us most about Good Manufacturing Practice — answered in short.

Good Manufacturing Practice is used to keep regulated products consistent, safe, and traceable. It shapes how teams write procedures, train people, record production, manage deviations, and prove control during audits. Companies rely on it in pharma, biotech, medical devices, food, and cosmetics.

GMP is the broad term for good manufacturing practice, while cGMP usually means current good manufacturing practice. EU GMP is the European framework many sites in Europe follow, especially in pharma and related industries. The terms overlap, but the exact expectations can differ by market and product type.

A strong Good Manufacturing Practice specialist often brings quality assurance, validation, documentation control, and audit support skills. Familiarity with SOPs, CAPA, change control, risk management, and production workflows is also important. For technical sites, experience with clean rooms, process validation, and computer system validation can matter too.

Good Manufacturing Practice projects can be small or very demanding, so the right level depends on the task. A document review or SOP cleanup may need a focused specialist, while a remediation program or inspection prep usually calls for deeper cross-functional experience. The key is proven work in regulated environments, not just theoretical knowledge.

Good Manufacturing Practice freelancers are useful when internal teams are tied up with production, audits, or launch work. They also help when a company needs short-term expertise for a gap assessment, an inspection response, or a temporary quality role. This is often the fastest way to add targeted capacity without long onboarding.

Good Manufacturing Practice work can be both remote and on-site. Remote support fits document control, SOP creation, training material, and audit preparation, while on-site work is better for plant walkthroughs, line support, and direct coordination with operations. Many projects use a mix of both.

A strong Good Manufacturing Practice specialist can explain how they improved control, documentation, or audit readiness in real projects. Look for clear examples of deviation handling, CAPA work, validation support, and cross-team coordination. Good specialists speak plainly, ask about the process, and focus on practical compliance rather than jargon.

Good Manufacturing Practice work in Frankfurt may involve international teams, site visits, and strict document control. Freelancers should be ready to work with local quality teams, handle English and sometimes German documentation, and adapt to the site’s specific procedures. Comfort with regulated environments and careful communication matters more than a generic CV.

The average hourly rate of freelancers in Frankfurt, Germany who have used Good Manufacturing Practice in their recent projects is 111 €, which corresponds to a daily rate of about 888 € based on an 8-hour working day.

Of the freelancers in Frankfurt, Germany who have used Good Manufacturing Practice in their recent projects, 90% hold at least a Bachelor's degree, 50% hold at least a Master's degree, and 10% hold a doctorate.

On average, freelancers in Frankfurt, Germany who have used Good Manufacturing Practice in their recent projects have 20 years of professional experience, with a single engagement typically lasting around 2.2 years.

The most common languages among freelancers in Frankfurt, Germany who have used Good Manufacturing Practice in their recent projects are German (100%), English (100%), and French (40%).

The most common industries among freelancers in Frankfurt, Germany who have used Good Manufacturing Practice in their recent projects are Pharmaceutical (80%), Healthcare (70%), and Information Technology (50%).

The most common business areas among freelancers in Frankfurt, Germany who have used Good Manufacturing Practice in their recent projects are Quality Assurance (90%), Product Development (70%), and Project Management (70%).

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.

Berlin Hamburg Munich Cologne Frankfurt Stuttgart Dusseldorf Leipzig Dortmund Essen Bremen Dresden Hanover Nuremberg

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Philipp Thomaschewski

FRATCH CEO

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