Cleanroom Technology Experts in Switzerland
matched in minutes from over 15,000 CVsHire experts who design contamination-controlled spaces, qualify HVAC and filtration systems, and manage validation documentation for regulated production. FRATCH connects you quickly with vetted, available freelancers whose experience fits your technical and compliance requirements.
Meet FRATCH Experts in Switzerland, who have recently used Cleanroom Technology
Veit M.
Last position:
Test Method Development and Validation Engineer at Gebr. Renggli AG
- Test method validation for destructive testing (peel-force testing) according to ASTM F88/F88M
Oliver W.
Last position:
Specialist Planner / Cleanroom Planning Lead at Major Aircraft Manufacturer
- Start-up and commissioning of the cleanroom
- Certification of the cleanroom
Hans S.
Last position:
Interim Manager, Consultant, Facilitator at Business Excellence Services GmbH
Interim manager, consultant, facilitator
Project management with focus on trouble shooting & customer care and/or product development/reengineering; regulatory management
Supply chain; risk and quality management; people management
Experienced within medical device; aerospace; packaging; small- & large equipment; optical- & electrical-systems; metal & plastics; free auditor
Since 2016, working for various accredited organizations as a freelance auditor regarding systems according to ISO 13485 and ISO 9001
2023-2024: Medical device product development, supply-chain and regulatory set-up with regard to a medical device re-engineering/launch and manufacturing
2023-2024: Project trouble shooter & customer care in the European aerospace industry within precision optics systems manufacturing; project risk and validation management including software validation
2022: Validation (FMEA, IQ OQ, PQ) management assigned with design and process risk assessment of complex electrical (IEC60601-1) mechatronics robots for MDR approval following ISO 14971
2022: Interim head of QM in aluminum-foil deep drawing process improvement; people and international Nespresso supplier quality management
2021-2022: Cytiva Cell Therapy greenfield project; assigned with design and implementation support of a certification, validation, GMP commissioning strategy for the technical infrastructure, e.g., clean rooms
2020-2021: Interim QA-Leader in Denmark assigned with the software release, manufacturing and distribution of Class IIb laser equipment for Candela, including international notified body and manufacturing transfer project
2020: Quality support and interim quality management for a manufacturer in the IVD test equipment supply chain and dialysis supplies in Bavaria
2018-2020: Expert/SME in Q-Management/Q-Engineering for orthopedic and arthroplasty device and tool production: turning, milling, cleaning, surface treatment and sterile packaging
2017: Re-engineering of the Medela product development process regarding cGMP 21CFR820.30/ISO 13485:2016 and MDR design control requirements for soft and hardware design regarding Class IIb pumps
2017: MDSAP preparation support and mock-audit coaching
2016: Interim senior QE-Expert for Maquet extracorporeal circulation devices manufacturing as ISO 14971 risk and change management expert in a Roche CAPA remediation and compliance project of IVD blood analyzers/gas sensor production
2016-2017: Orthopedic and arthroplasty implants design history file (DHF) review regarding compliance to 21 CFR 820.30 design control requirements
2015: Assigned by Novartis with design control for a new parenteral drug delivery system; manufacturability assessments during design evaluation; assessing potential plastic injection molding and/or high-volume assembly contractors in Europe and the US
2014: Assessing/auditing metallurgy process validation (IQ/OQ/PQ) of Zimmer contract manufacturers around Europe for FDA audit readiness; Depuy-Synthes subject matter expert (SME)
2013-2014: CAPA-8D process reengineering and setting in place/training new EtQ software tools; coaching of project and product managers in working through individual CAPAs; remediation of global legacy CAPAs; supporting complaint and field action (FSCA) management
2012-2013: QA/RA Manager at Sias AG for in vitro diagnostics (IVD) liquid handling robots manufacturing; led small team for electrical safety CE/CB scheme product approvals; QMS, change and CAPA management
2011-2012: Site Quality Manager at Medtronic for drug eluting balloon and Nitinol stent-catheter manufacturing; quality operations including Q-engineering and control; led 15 direct and indirect reports
2009-2010: Supported quality initiatives in medical device industry; assessments and audits for manufacturers and suppliers as a consultant of Business Excellence Services
Robert O.
Last position:
Interim SQM Plastics at thyssenkrupp Automotive, tkDC Dynamic Components
- Supplier management
- Carrying out SQI audits
- Supporting sustainability activities
Jürgen B.
Last position:
Design Engineer at LidroTec GmbH
- development of wafer manufacturing with cleanroom technology
- Tools: Inventor
Martin A.
Last position:
Martin Aicher
Main areas of activity ⋅ Martin Aicher
Areas of expertise
Medical technology
Sensor technology
Technical optics
Mechatronics
Microsystems technology
Biocompatible materials
Implants and endoprosthetics
Project management
Quality management IPMA
Regulatory affairs
Education
Dr.-Ing. Medical Technology
M.Sc. Medical Technology
Dipl. Ing. (FH) Medical Technology
Surgical mechanic, precision mechanic
Methodical product development
26 years of research, development, verification and agile product development
5 years of hands-on manufacturing of micromechanical instruments and implants
Projects
Development and verification of technical optics
Microscopy
Endoscopy
Immersion optical systems
Optical sensors
Light guides
Device development — medical electronics, active medical devices
Electromagnetic therapy devices for microcirculation of blood vessels
Electric drives, precision mechanics motors
Embedded devices, Medicine 4.0 / Industry 4.0
Feasibility studies, prototype design, electromechanical, chemical and hydrodynamic characterization up to series maturity
Structural integration of motors for pump systems
Integration of motors for catheter drives
Implantable drive systems with motors
Bone saws with Maxon motors
Osteosynthesis implant (bone implant) with linear drive
Electromagnetic therapy devices for microcirculation of blood vessels
Gold and platinum substitution for electrodes
Electrochemical impedance spectroscopy (EIS)
Characterization and development of battery cells and Li-ion batteries
Biocompatible materials: stainless steel, titanium, nitinol, polymers, ceramics, composites
Vacuum device with pumps for wound healing
Braided tubes (reinforced hoses)
Shaft instruments and trocars
Surgical instruments, minimally invasive instruments (MIC)
Analytical instruments, sensors and fluid preparation
Monitoring systems
In vivo diagnostics (IVD)
Inline measurement systems for monitoring and analytical devices
Feasibility studies, prototype design, electrochemical and hydrodynamic characterization up to series maturity
Electrochemical deionization (EDI) as a monitor
Membrane technology
Measurement method and control of carbide saturation in cooling water
pH sensor
Optical sensors with laser diodes and LEDs
Dissolved O2 sensor
CO2 sensors
Ion-selective sensor (ISE)
Conductivity sensors
Turbidity sensor according to ISO 7027
Biosensors
Flow and pressure sensors
Gold and platinum substitution for electrodes
Electrochemical impedance spectroscopy (EIS)
Biocompatible materials: stainless steel, titanium, nitinol, polymers, ceramics, composites
Design of plastic injection-molded components and housings
Calculation and design of fluid channels
Design of metal die-cast components
Design of sheet metal parts
Implants and prostheses
Endoprosthetics: knee and hip endoprostheses
Bypass implants
Nitinol stents
Bone plates
Dental implants
Precision meshes
Instruments for medical technology
Angioplasty: PTCA percutaneous transluminal coronary angioplasty with balloon catheter
Catheter system as minimally invasive heart pump
EN ISO 10555-4: intravascular catheters
Braided tubes (reinforced hoses through precision meshes)
Thrombectomy with rotablation catheter
Trocars
Surgical instruments, minimally invasive instruments (MIC)
Endoscopes ISO 8600-1, EN 60601-2-18, EN 62471
Regulatory affairs for medical devices
CE for Europe (Class II and III), EU Medical Device Regulation 2017/745 (MDR)
EU Regulation 2017/746 for in vitro diagnostics (IVDR)
Ensuring complete documentation according to current regulatory requirements
FDA registration and approval 510(k), PMN, PMA, Class II, III
Design History Files (DHF), Device Master Record (DMR), Device History Record (DHR)
Internal and external audits
FDA and CE audits
Mock audits
Requirement engineering, user requirement specifications, functional requirement specifications
Quality management and relevant standards for medical technology
EN ISO 9001:2015
EN ISO 13485:2021
USA FDA 21 CFR 820 Quality Management System
FDA 21 CFR §§ 803, 806, 807, 830
In vitro diagnostics (IVD, IVDR) FDA 21 CFR §§ 600, 610, 660
USA FDA risk management for medical devices DIN EN ISO 14971:2019
P-FMEA for production
Usability of medical devices EN 62366-1:2021
CAPA (Corrective and preventive action) and GMP
Medical electrical equipment EN 60601-1:2013
EMC for medical devices DIN EN 60601-1-2:2022
Medical device software EN 62304:2018
Cell culture in cleanroom with different cell lines for biocompatibility testing of polymers and alloys
Biological evaluation of medical devices EN ISO 10993
Clinical investigation of medical devices ISO 14155
Manufacturing technology and processes
Process qualification and validation
Injection molding technology
CNC micromechanical manufacturing
Microsystems technology, printed circuit boards (PCB)
Joining technologies: laser welding of titanium, stainless steel, plastics as well as gluing and ultrasonic welding
Evaluation, setup and qualification of equipment
Thin film and surface technology
Coating of implants and tribological surfaces with chemical vapor deposition (CVD) and physical vapor deposition (PVD), sputtering of precious metals, stainless steels, nitinol, titanium alloys, polymers and ceramics
Plasma technology for functional coatings: hydrophilic and hydrophobic surfaces
Nanotechnology: surface functionalization: self-assembled monolayers (SAM)
Product Life Cycle Management
Finite element method
ANSYS FEM
Structural mechanics, statics
Fluid mechanics, flow simulations
Electrical engineering, electromagnetic fields
Characterization and testing of microelectronics
PCB (printed circuit board)
Sensor technology
Microcontrollers
CAN bus: ISO 11898, SAE
Control and data management with LabVIEW and Matlab
Programming language
Python 3.14
CAD
Autodesk Inventor
Pro/ENGINEER, PTC Creo Parametric
SolidWorks
Siemens NX
Solid Edge
Standards-compliant technical drawings
Endurance tests, mechanical, fluid mechanical, electrical and chemical characterization
Verification, V-Model, End of Line (EOL) testing
Writing work instructions for production, English regulatory documents and scientific articles
Support of clinical studies
Data processing, digital data management and statistics
Professional handling of Microsoft Office applications: PowerPoint, Word and macro programming for Excel
© 2026 M. Aicher
Axel K.
Last position:
Project Manager and Owner's Representative in Technical Trades at Carl Zeiss AG
- New factory buildings, ISO5 cleanroom
- Oberkochen
- Construction cost EUR 1.2 billion
Discover over 15,000 top freelancers
Statistics of experts using Cleanroom Technology
Aggregated from the professional profiles of matched freelancers.
Experience
34 years
Position duration
3.2 years
Positions per freelancer
20
Top business areas
Quality Assurance, Product Development, Project Management
Top industries
Healthcare, Manufacturing, Aerospace and Defense
Certification focus areas
Quality Assurance, Product Development, Information Technology
Bachelor's degree or higher
83%
Master's degree or higher
67%
Doctorate
50%
Certifications per freelancer
3
Most common languages
German, English, French
Speak two or more languages
100%
Based on our profile pool as of 10 Sep 2026.
Daily rate distribution
The chart shows how the daily rates of freelancers in this technology in Switzerland 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 Switzerland using Cleanroom Technology
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 10 Sep 2026. Actual rates may vary depending on seniority level, experience, skill specialization, project complexity, and engagement length.
Cleanroom Technology experts industry focus
See which industries our matched freelancers work in most often — every figure is calculated live from the freelancers on FRATCH.
- Healthcare (100%)
- Manufacturing (100%)
- Aerospace and Defense (57%)
- Pharmaceutical (57%)
- Construction (43%)
- Automotive (29%)
- Chemical (29%)
- Education (29%)
Please note that freelancers can work across multiple industries, so percentages overlap.
About the technology
Controlled environments
Cleanroom Technology creates spaces where airborne particles, microorganisms, temperature, humidity and pressure remain within defined limits. Companies use it to protect sensitive products, processes and people during manufacturing, testing and research. The discipline combines room design, air treatment, filtration, monitoring and operating procedures.
Where it is used
Cleanrooms support work in pharmaceutical production, biotechnology, medical devices, semiconductor manufacturing, aerospace, food processing and advanced laboratories. Their design depends on the required cleanliness level, process risk, personnel flow, material flow and cleaning method. In Switzerland, regulated life sciences and precision manufacturing often require close coordination between facility, quality and production teams.
- Plan classified rooms and controlled zones
- Protect sterile or particle-sensitive processes
- Separate personnel, materials and waste flows
- Establish pressure cascades and recovery targets
Systems and tooling
A cleanroom project can involve HEPA or ULPA filtration, air-handling units, fan-filter units, airlocks, pass-throughs, isolators and restricted-access barriers. Specialists work with building management systems, environmental monitoring, particle counters and data historians. They also use risk assessments, commissioning plans, qualification protocols and controlled documentation.
Project expertise
Companies bring in freelance expertise when they need a new facility, a line extension, a retrofit or support during an audit. Professionals can define user requirements, review layouts, coordinate suppliers and prepare commissioning and qualification activities. They may also investigate deviations, optimise airflow and improve cleaning or gowning procedures without interrupting critical operations.
- Translate process needs into room and HVAC requirements
- Coordinate mechanical, electrical and process interfaces
- Prepare validation evidence and handover records
- Support change control and deviation investigations
What strong specialists know
Strong professionals understand both contamination control and the process taking place inside the room. They can explain how airflow patterns, pressure differences, filtration, materials and personnel behaviour affect product quality. They distinguish design assumptions from measured results and keep decisions traceable through drawings, protocols, reports and standard operating procedures.
Choosing the right fit
The right specialist depends on the assignment: concept design, HVAC integration, qualification, environmental monitoring, quality documentation or operational improvement. Look for experience with the relevant product risk, room classification and regulated environment rather than cleanroom terminology alone. For Swiss projects, agree early on site presence, coordination with local contractors and the working languages needed for documentation and daily collaboration.
Frequently asked questions
The facts hiring teams ask for most often when it comes to Cleanroom Technology.
Cleanroom Technology controls airborne contamination and environmental conditions in spaces used for sensitive production, research or testing. It helps protect medicines, medical devices, microelectronics, biological materials and other products from particles, microorganisms and process variation.
Cleanroom Technology goes beyond ordinary heating, ventilation and air conditioning. It combines controlled airflow, filtration, pressure relationships, monitoring, cleaning procedures and documented qualification to meet a defined process or product risk.
A strong Cleanroom Technology specialist may also understand HVAC design, building management systems, environmental monitoring, validation, quality assurance and contamination-control strategy. Experience with GMP documentation, risk assessment and commissioning is especially useful for regulated facilities.
The required depth depends on the assignment. A specialist supporting qualification or remediation should have handled comparable rooms, systems and documentation, while a smaller monitoring or procedural task may need narrower expertise. Ask for examples that match the process risk and project phase.
Cleanroom Technology planning, document review and protocol writing can often be done remotely. Surveys, commissioning, airflow checks, training and issue resolution usually benefit from on-site work in Switzerland, with the exact balance agreed before the engagement.
Check whether the specialist has worked with the relevant cleanliness requirements, production process and validation framework. Ask how they record assumptions, handle deviations and communicate with facility, quality and operations teams. Clear evidence is more useful than a generic list of room types.
Cleanroom Technology is the broader discipline used to control contamination and environmental conditions. A sterile manufacturing facility applies those principles alongside aseptic processes, sterilisation controls, microbiological methods and strict quality systems; not every cleanroom is designed for sterile production.
A Cleanroom Technology specialist should be able to write clear technical and qualification documents in the language required by the project. English is common in international life-science teams, while German, French or Italian may matter for local coordination, contractors and site procedures.
The average hourly rate of freelancers in Switzerland who have used Cleanroom Technology in their recent projects is 140 €, which corresponds to a daily rate of about 1,118 € based on an 8-hour working day.
Of the freelancers in Switzerland who have used Cleanroom Technology in their recent projects, 83% hold at least a Bachelor's degree, 67% hold at least a Master's degree, and 50% hold a doctorate.
On average, freelancers in Switzerland who have used Cleanroom Technology in their recent projects have 34 years of professional experience, with a single engagement typically lasting around 3.2 years.
The most common languages among freelancers in Switzerland who have used Cleanroom Technology in their recent projects are German (100%), English (100%), and French (43%).
The most common industries among freelancers in Switzerland who have used Cleanroom Technology in their recent projects are Healthcare (100%), Manufacturing (100%), and Aerospace and Defense (57%).
The most common business areas among freelancers in Switzerland who have used Cleanroom Technology in their recent projects are Quality Assurance (86%), Product Development (71%), and Project Management (71%).
Main locations of FRATCH Experts, who have recently used Cleanroom Technology
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:
- Germany
- Switzerland
Zurich Geneva Basel Bern Request a free demo
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FRATCH CEO
