Good Manufacturing Practice Experts in Vienna
matched in minutes by AIHire experts who design GMP quality systems, qualify equipment and prepare facilities for audits across pharmaceutical, biotechnology, medical device and food production. FRATCH connects you with vetted, available freelancers through fast, precise matching.
Meet FRATCH Experts in Vienna, who have recently used Good Manufacturing Practice
Jori M.
Last position:
Agile IT Manager Healthcare Systems at MA01 Gov. Digital City
- Responsible for managing GMP-Critical systems
- Leading team of 20 professionals
- Vendor management with €15 M annual budget
Lorenz G.
Last position:
Business Analyst at Wirtschaftsagentur Wien
- Conducting a feasibility study on introducing an in-house DWH as a central data source
- Conducting workshops for current state analysis (processes, reports, KPIs) together with the clients
- Gathering and detailing business requirements including a target concept for an in-house DWH
- Coordinating and clarifying data deliveries and interfaces in meetings with stakeholders and data providers
- Developing initial data models as a basis for data quality and later implementation
- Drafting solution variants including architecture and operation options and decision basis
- Creating the business case including effort estimates, cost-benefit analysis, and decision report
Alexander H.
Last position:
QMS Senior Specialist at Abbott GmbH
- Conducted technical QMS assessments of the corporate complaints platform
- Estimated effort for the upgrade activity
- Developed a high-level data migration plan
- Coordinated with the software vendor on required adjustments
- Developed a proof of concept and presented it to business stakeholders
Michael P.
Last position:
Strategy Consultant & Program Architect at Hypo Tirol Bank AG
- Portfolio Analysis & Migration Roadmap: Conducted structured analysis and risk classification of the HCL Notes infrastructure, created a prioritized migration portfolio with effort estimates as a key decision basis for management.
- Target Architecture & Modernization Concept: Developed the architecture strategy for retiring legacy applications, defined requirements for a centralized business process engine to reduce OPEX and licensing costs in the long term.
- Program Governance & Setup: Established roadmap and backlog structures as well as central project documentation (MS SharePoint), set up stakeholder management for the Notes decommissioning program.
Veronika H.
Last position:
Manufacturing Lead at GI.HU (Genetic Immunity) Kft.
- Technology and operational leader for R&D and GMP manufacturing and contract manufacturing activities of the product candidate
- Successful screening and selection of CMOs and CDMOs, establishment of workflows
- Completed risk assessments and gap analyses in relation of the production activities
- Acting as key contact point for CMOs, CDMOs and other contractors; managing and leading negotiations
- Analysis of the current technology of the product candidate (drug substance with biotechnological origin, excipient polymer and related nano formulation) and the medical device; technology optimization, critical parameter setting
- Technology related gap- and risk analysis, decision management, project management and prioritization
- Crisis management and solution setup by critical parameter analysis and investigation of critical quality attributes of the processes
- Definition and selection of the related and needed quality control setup (evaluation of QC tests, specification set up according to relevant guidelines)
- GMP related activities: deviation, change control and OOS management, compilation of GMP related documentation (SOP, WI, etc.)
Peter K.
Last position:
Sabbatical
Discover over 15,000 top freelancers
Statistics of experts using Good Manufacturing Practice
Aggregated from the professional profiles of matched freelancers.
Experience
17 years
Position duration
1.8 years
Positions per freelancer
12
Top business areas
Information Technology, Project Management, Product Development
Top industries
Information Technology, Banking and Finance, Healthcare
Certification focus areas
Project Management, Information Technology, Product Development
Bachelor's degree or higher
80%
Master's degree or higher
80%
Certifications per freelancer
3
Most common languages
German, English, Russian
Speak two or more languages
83%
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 Vienna 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 Vienna 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.
- Information Technology (67%)
- Banking and Finance (50%)
- Healthcare (50%)
- Pharmaceutical (50%)
- Government and Administration (50%)
- Biotechnology (33%)
- Chemical (33%)
- Transportation (33%)
Please note that freelancers can work across multiple industries, so percentages overlap.
About the technology
GMP foundations
Good Manufacturing Practice, commonly abbreviated as GMP, is the framework for producing medicines, active substances, medical products and other regulated goods consistently and safely. It covers facilities, equipment, materials, processes, records and people. The goal is controlled quality from incoming materials through release and distribution, with evidence for every critical decision.
Regulated production
GMP expertise appears wherever contamination, mix-ups, errors or undocumented changes could affect product quality or patient safety. Typical assignments include:
- Designing pharmaceutical and biotechnology quality systems
- Preparing sterile, non-sterile and biologics manufacturing areas
- Establishing controls for active pharmaceutical ingredients
- Supporting medical device and combination-product operations
- Improving batch records, deviations and product release
Systems and tools
Professionals work with quality management systems, electronic batch records, document control, training management and laboratory information systems. Their work may include process validation, cleaning validation, computerised system validation, equipment qualification and data integrity controls. They also apply risk management, change control, CAPA and supplier qualification across the quality system.
When specialists help
Companies bring in freelance GMP specialists during facility start-up, technology transfer, remediation and inspection preparation. They can close a gap in quality leadership, review procedures, lead validation work or strengthen operations before a product launch. In Vienna, collaboration may combine remote documentation and analysis with on-site work in production, laboratory or warehouse areas.
Evidence and compliance
Strong professionals connect requirements to practical controls and clear records. They understand how to interpret EU GMP expectations, Good Distribution Practice, ICH guidance and applicable national requirements without treating compliance as paperwork alone. They can investigate deviations, identify root causes, assess risks and make sure corrective actions remain effective.
Choosing the right expert
Look for evidence of work in a comparable product, process and regulatory setting. A capable specialist explains how they controlled contamination, validated a process, handled an audit observation or protected data integrity. They should communicate clearly with production, quality control, engineering and management teams, and distinguish a proportionate control from unnecessary complexity.
Frequently asked questions
Questions about Good Manufacturing Practice? Start with the answers below.
Good Manufacturing Practice is used to control how regulated products are made, tested, stored and released. It ensures that processes are repeatable, records are reliable and quality risks are addressed before products reach customers or patients.
GMP is a product- and process-focused framework for regulated manufacturing, while quality assurance is the broader system that manages confidence in quality. ISO standards can support a quality system, but GMP adds detailed expectations for production controls, batch records, validation, hygiene and release decisions.
A strong Good Manufacturing Practice specialist often combines quality systems with validation, deviation investigation, CAPA, audit readiness and data integrity. Experience with electronic quality systems, laboratory operations, process engineering or regulatory submissions can also be valuable, depending on the assignment.
The right level depends on the risk, product stage and scope of the work. A focused procedure review may need a specialist familiar with the relevant operation, while remediation, sterile manufacturing or inspection preparation calls for someone who has led comparable activities from assessment through documented closure.
Good Manufacturing Practice work can often be handled remotely when it involves document review, risk assessments, training content or quality-system design. Equipment qualification, process observation, sampling and facility assessments usually require site access. In Vienna, teams commonly combine remote work with planned on-site sessions.
Ask for specific examples involving the same product type, manufacturing process and regulatory environment. Review how the specialist approached deviations, validation, audit findings and documentation, and check whether they can work effectively with quality, production, laboratory and engineering teams.
Good GMP deliverables are clear, traceable and usable by the people who must follow them. Procedures should reflect the real process, validation should link evidence to acceptance criteria, and investigations should show a defensible root cause, risk assessment and effective action.
A Good Manufacturing Practice specialist working in Austria should understand the applicable EU GMP framework and how it affects the product and facility involved. They should also be comfortable coordinating with local teams, documenting work in the agreed language and meeting site-access and confidentiality requirements.
The average hourly rate of freelancers in Vienna, Austria who have used Good Manufacturing Practice in their recent projects is 119 €, which corresponds to a daily rate of about 951 € based on an 8-hour working day.
Of the freelancers in Vienna, Austria who have used Good Manufacturing Practice in their recent projects, 80% hold at least a Bachelor's degree and 80% hold at least a Master's degree.
On average, freelancers in Vienna, Austria who have used Good Manufacturing Practice in their recent projects have 17 years of professional experience, with a single engagement typically lasting around 1.8 years.
The most common languages among freelancers in Vienna, Austria who have used Good Manufacturing Practice in their recent projects are German (100%), English (83%), and Russian (50%).
The most common industries among freelancers in Vienna, Austria who have used Good Manufacturing Practice in their recent projects are Information Technology (67%), Banking and Finance (50%), and Healthcare (50%).
The most common business areas among freelancers in Vienna, Austria who have used Good Manufacturing Practice in their recent projects are Information Technology (100%), Project Management (100%), and Product Development (83%).
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:
Vienna 
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