Good Manufacturing Practice Experts in Austria
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Meet FRATCH Experts in Austria, who have recently used Good Manufacturing Practice
Stavros V.
Last position:
Transformation & Change Lead (Freelance) at Sanofi
- Led the global transformation of Talent Operations by inhousing recruitment technologies, processes, and teams, reducing over 20 external partners to 2, defining the strategy to hire hundreds of internal talent specialists, and redesigning organisational structures and processes worldwide.
- Drove gap analyses and impact assessments and led the global rollout of Beamery, HireVue, and Paradox, covering solution design, pilot markets, global deployment, and hypercare, ensuring smooth market transitions and standardised operations.
- Developed and maintained detailed project plans, timelines, milestones, RAID logs, and governance routines, leveraging SharePoint as the central platform for programme documentation, rollout artefacts, approvals, and decision tracking.
- Coordinated cross-functional stakeholders including HR, IT, regional teams, and external vendors, using SharePoint-based documentation and governance frameworks to align requirements, manage dependencies, and resolve delivery issues.
- Conducted gap analyses and impact assessments across Paradox, Beamery, and Workday to ensure pilot readiness and global launch success, with outputs captured and governed through SharePoint.
- Built and executed comprehensive change management plans using ADKAR methodology, covering stakeholder mapping, communications, training, and adoption activities, supported by SharePoint-hosted enablement materials and rollout documentation.
- Broke down silos across regions and functions to drive adoption of new systems, processes, and ways of working.
- Tracked adoption metrics and user feedback post-deployment, driving continuous improvement in user experience and operational performance.
Herbert F.
Last position:
Pentest Center of Excellence - Strategy & Implementation at Cybersecurity & IT Risk Managed Services
- Built board/management business-case scenarios; assessed services, vendors, contracts and financials; defined target operating model, service catalogue, organization, processes and tooling.
- Implemented near-shore CoE in Romania and supported rollout to an international insurance group
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
Albert S.
Last position:
Managing Director & Owner at Metatron Industrial Solutions GmbH
- Responsible for strategy, technological development, and execution in industrial plant engineering — with a focus on extrusion technology and AI-driven process optimization
- Freelance project execution for international clients (e.g. BĂĽhler, Enercon, Bayer, Elanco)
- Development of proprietary AI-powered software solutions for production control and environmental technologies
- International project leadership for clients in the food, pharmaceutical, and chemical industries; active involvement in building deep-tech start-ups and selective investments in Industry 4.0, cleantech, and AI manufacturing
- Details see attachment “Albert_Schiller_References_Industrial_Projects”
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
Manuel K.
Last position:
Overall project manager for the global roll-out of a quality and document management system at International medical device company
- Took over overall project leadership after the roll-out was stopped the previous year
- Identified causes and planned a new approach
- Organized and conducted qualification tests of new software versions
- Planned and coordinated all tasks and assignments at six sites worldwide and with the software provider
- Aligned compliance topics with the quality heads at the sites
- Organized and held steering committee meetings to report to management
- Successful go-live in fall 2024
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.
Michael S.
Last position:
Director, IT at Austria Juice GmbH
- Directed IT operations across 13 sites in China, Romania, Poland, Hungary, Germany, Ukraine, and Austria.
- Built and led a new IT team with personnel based in Poland, Hungary, Romania, and Germany.
- Upgraded outdated IT infrastructure at sites in Austria, Germany, Romania, and Poland, enhancing clients, printers, networks, servers, storage, firewalls, and backups.
- Retired the legacy phone system and transitioned to Teams.
- Established and deployed AI tools, including Copilot and Zapier.
- Implemented NIS II readiness and achieved ISO 27001 certification.
- Eliminated inefficient business applications to enhance operational efficiency.
- Developed and executed new processes for operations technology, business process outsourcing, purchasing, human resources, and IT.
- Launched a new SAP Warehouse System.
- Established IT standards across all sites.
- Engaged effectively with internal and external stakeholders.
- Defined and monitored security KPIs, ensuring targets were met.
- Managed budgeting processes, achieving a 15% reduction in operational expenditure.
Jori M.
Last position:
Agile IT Manager Healthcare Systems at MA01 Gov. Digital City
- Responsible for managing GMP-critical systems
- Leading a team of 20 professionals
- Vendor management with a €15M annual budget
Stefan W.
Last position:
Corporate IT Project Manager at OctaPharma
- SAP rollout to multiple locations of the company
- Predictive project management
- Functional stream lead
- Coordination of 17 streams
- Data migration support
- Cutover management (go live)
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
Georg J.
Last position:
Owner & CEO / Senior IT-Consultant at CONPITEC GmbH
- CONPITEC offers premium consulting and IT services.
- Our clients are leading global IT service providers, as well as international groups in the pharmaceutical industry in Europe.
Discover over 15,000 top freelancers
Statistics of experts using Good Manufacturing Practice
Aggregated from the professional profiles of matched freelancers.
Experience
20 years
Position duration
2 years
Positions per freelancer
11
Top business areas
Information Technology, Project Management, Product Development
Top industries
Information Technology, Pharmaceutical, Healthcare
Certification focus areas
Information Technology, Project Management, Quality Assurance
Bachelor's degree or higher
75%
Master's degree or higher
75%
Certifications per freelancer
4
Most common languages
German, English, Spanish
Speak two or more languages
92%
Based on our profile pool as of 19 Sep 2026.
Daily rate distribution
The chart shows how the daily rates of freelancers in this technology in Austria 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 Austria 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 19 Sep 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 (85%)
- Pharmaceutical (69%)
- Healthcare (46%)
- Banking and Finance (38%)
- Food and Beverage (38%)
- Manufacturing (38%)
- Biotechnology (31%)
- Transportation (31%)
Please note that freelancers can work across multiple industries, so percentages overlap.
About the technology
Quality Standards in Regulated Manufacturing
Good Manufacturing Practice, commonly known as GMP, forms the regulatory framework ensuring pharmaceuticals, medical devices, and biologics meet rigorous safety criteria. In Austria, life science facilities align operations with both European Union guidelines and national oversight. Establishing robust controls prevents contamination, batch failures, and compliance deviations.
Core Technical Capabilities and Tooling
Independent specialists configure validation frameworks, maintain data integrity standards, and audit computerized systems:
- Computerized system validation under GAMP 5 principles
- Cleanroom classification and environmental monitoring protocols
- Quality Management Systems adhering to EU GMP Annex 1 and Annex 11
- Deviation management, root cause analysis, and CAPA workflows
- Sterilization, aseptic processing, and cleaning validation
Delivering Compliance for Austrian Facilities
Austria serves as a central European hub for biomanufacturing, active pharmaceutical ingredient synthesis, and medical engineering. Projects across biotech hubs in Vienna and Upper Austria require swift integration of regulatory standards. External specialists ensure local manufacturing sites satisfy national safety bodies and international markets.
Driving Complex Remediation and Audit Success
External experts bring clarity when manufacturing pipelines experience critical quality deviations or scheduled regulatory assessments. They bridge operational shop-floor practices with meticulous documentation standards. Their intervention minimizes batch rejections and accelerates approvals during tech transfers and facility commissionings.
Prerequisites for High-Impact GMP Engagements
Organizations engage external professionals when internal quality assurance teams face tight launch schedules or regulatory findings:
- Production scaling demands qualification of new processing lines
- Urgent preparation required for upcoming official inspections
- Introduction of automated enterprise systems requiring strict validation
- Backlogs in CAPA resolutions and standard operating procedure updates
Traits of Top Regulatory Manufacturing Specialists
Exceptional practitioners balance hands-on shop floor pragmatism with rigid adherence to documentation. They master risk management frameworks such as ICH Q9 and communicate fluidly between engineering, laboratory, and quality teams. Their technical insight turns compliance into an operational advantage rather than an organizational burden.
Frequently asked questions
Curious about Good Manufacturing Practice? Here are the answers that come up again and again.
An expert in Good Manufacturing Practice designs, validates, and audits production processes to ensure products meet strict regulatory quality standards. They establish Standard Operating Procedures, handle non-conformances through CAPA processes, and ensure cleanroom operations satisfy formal guidelines like EU GMP.
While ISO 9001 provides general quality management principles and GLP governs non-clinical safety testing, GMP applies specifically to commercial-scale manufacturing of therapeutic products. It enforces legally binding standards for hygiene, traceability, process validation, and personnel qualification to protect patient health.
Specialists working in cGMP environments regularly operate Enterprise Resource Planning platforms, Laboratory Information Management Systems, and electronic Quality Management Systems. They validate these setups under GAMP 5 and Annex 11 standards to ensure electronic records and signatures remain fully compliant.
Documentation audits, protocol drafting, and validation plan authoring can be performed remotely. However, facility walkthroughs, equipment qualification, and Austrian regulatory inspection support usually require targeted on-site presence at production plants across regions such as Vienna, Tyrol, or Styria.
Deliverables include Installation, Operational, and Performance Qualification protocols alongside summary reports. A professional specializing in Good Manufacturing Practice also produces risk assessments, standard operating procedures, validation master plans, and detailed deviation remediation files.
Technical documentation and validation protocols in international facilities are frequently authored in English. However, working directly with shop-floor operators and addressing national inspectors in Austria often requires business-fluent German proficiency alongside thorough knowledge of EU GMP directives.
Examine their track record with successful agency audits, facility certifications, and method transfers. Strong practitioners in current Good Manufacturing Practice demonstrate direct familiarity with relevant annexes, specific dosage forms, and cleanroom automation.
Vetted professionals adapt rapidly due to standard industry frameworks. Once oriented with the site validation master plan and existing Quality Management System, an expert in Good Manufacturing Practice delivers compliant documentation and provides process oversight within days.
The average hourly rate of freelancers in Austria who have used Good Manufacturing Practice in their recent projects is 123 €, which corresponds to a daily rate of about 985 € based on an 8-hour working day.
Of the freelancers in Austria who have used Good Manufacturing Practice in their recent projects, 75% hold at least a Bachelor's degree and 75% hold at least a Master's degree.
On average, freelancers in Austria who have used Good Manufacturing Practice in their recent projects have 20 years of professional experience, with a single engagement typically lasting around 2 years.
The most common languages among freelancers in Austria who have used Good Manufacturing Practice in their recent projects are German (100%), English (92%), and Spanish (23%).
The most common industries among freelancers in Austria who have used Good Manufacturing Practice in their recent projects are Information Technology (85%), Pharmaceutical (69%), and Healthcare (46%).
The most common business areas among freelancers in Austria who have used Good Manufacturing Practice in their recent projects are Information Technology (92%), Project Management (92%), and Product Development (69%).
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.
Vienna Graz 
Vienna Countries:
- Germany
- Austria
- Switzerland
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