01.11.2025 aktualisiert

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Consultant - Life sciences

Biberist, Schweiz
Weltweit
Mechanical ingenieur
Biberist, Schweiz
Weltweit
Mechanical ingenieur

Profilanlagen

CV - Balazs Toth

Skills

BiologieSterilisationBestrahlungIso 13485ProjektmanagementMikrobiologieVerpackungstechnikPharmaverpackungenSimulationenVerkehrsbautenValidierungstestsProzess ManagementDesign Verification TestVerpackung und KennzeichnungValidierungsprotokolle
ISO 13485; ISO 13485 – internal auditor
Medical device packaging (ISO 11607-1 and -2; ASTM F1980, ASTM F1886, ASTM1929, ASTM F88, ASTM F2096, EN 868-5, EN 868-10)
Transport simulation (ASTM D4169)
Microbiology and sterile barrier system (ISO 15378, DIN-58953-6; DIN EN ISO 10993 1, ISO 10993-5, ISO 10993-7)
Sterilisation (EN ISO 11737-1 and -2; EN 14644; EN 556-1 and -2; ISO 11135; EN ISO 14161)
Member of the organisation: ASTM (American Society for Testing and Materials) Project management
4DX and 7 Habits (Franklin Covey)
EU Directives (93/42/EEC, 98/79/EC and 90/385/EEC) (MDD)
Regulation (EU) 2017/745 (MDR)
Agile project management

Sprachen

DeutschgutEnglischverhandlungssicherUngarischMuttersprache

Projekthistorie

Consultant: Bench Testing

Implantica

Pharma und Medizintechnik

50-250 Mitarbeiter

Responsibilities:
Gap analysis of sterile barrier system
Prepare the sterile barrier system bench testing plan: including extreme
environmental conditioning, shipment simulation, packaging and functional tests
Define the necessary unique distribution cycle (DC 2 according to ASTM D4169)
proper for the planned logistics
Define climate conditioning parameters depending on target market
Create sterile packaging standard implementations and summary document
Coordinate the bench testing process.
Define the packaging test methods and create test descriptions

Projects:
Testing of abdominal implant and its packaging system
Testing of injection tool and its packaging system for the abdominal implant

Consultant - MDR Remediation Specialist

Ypsomed AG.

Pharma und Medizintechnik

500-1000 Mitarbeiter

Responsibilities:
Gap analysis for sterilisation and sterile packaging
Coordinate the sterile barrier system developments
Risk analysis of the sterilisation and sterile barrier system
Define the sterilisation strategy of new products
Prepare the sterilisation and sterile packaging process validation plan
Prepare the sterilisation and sterile packaging Design Verification plan
Create sterile packaging standard implementations and summary document
Coordinate sterilisation and sterile packaging validation and verification
Define the packaging test methods and create test descriptions
Define the proper machines and tools for packaging tests
Calculate the EO residual limits after sterilisation for new products
Define microbiological limits (CFU limits) for new products
Define endotoxin test frequency and limits
Define physical contamination test frequency and limits

Projects:
Development of infusion sets for diabetes care
Development of ready-to-use patch injector
Development of insulin pump system

Engineering Manager

Medicontur Ltd.

Pharma und Medizintechnik

250-500 Mitarbeiter

Responsibilities:
Coordinate the daily work of the engineering and maintenance team (10 employees)
Ensure continuous production
Improve manufacturing process, implement LEAN concepts
Validation of new processes and equipment
NPI - transfer newly developed products/machines into the production

Consultant and Business Analyst

Asseco Central Europe H.

Industrie und Maschinenbau

250-500 Mitarbeiter

Responsibilities:
Optimisation of production process with plant simulation software
Real Time monitoring of material flow and production
Simulation, implementation and monitoring of material handling with AGVs
Clarify relevant customer requirements about the product
Market research for possible customers

Deputy - Head of Development Center

BBraun Medical Kft

Pharma und Medizintechnik

>10.000 Mitarbeiter

Responsibilities:
R&D responsible for wound drainage and suction devices
Substitute of the Head of Development Center in his absence
R&D responsible for medical device packages, whole portfolio produced on site
Coordinate projects, capacities and delegate tasks within the R&D group

Projects:
Update or prepare documents to be compliant according to the new MDR regulation
Development of new, crystal clear drain bottles with tube set to the US market
Packaging optimisation - define new materials, harmonise current portfolio
Coordination of packaging Process Validations and Design Verification based on ISO
11607-1/2
Re-validation of the EO sterilisation cycle
Prepare a new R&D lab - define layout, equipment, suppliers

Development Project Manager

BBraun Medical Kft

Pharma und Medizintechnik

>10.000 Mitarbeiter

Responsibilities:
R&D responsible for wound drainage and suction devices
R&D responsible for medical devices packages produced on site

Projects:
Packaging optimisation - define new materials, harmonise current portfolio
Coordination of packaging Process Validations and Design Verification based on ISO
11607-1/2
Development of new, crystal clear drain bottles with tube set to the US market
Supplier Audit - external lab
Ensure the clean water supply for production
Define frequency of testing and the sampling points of the clean water system
Prepare URS for new production equipment
Revise specifications and drawings of supplier.

Development Engineer

BBraun Medical Kft

Pharma und Medizintechnik

>10.000 Mitarbeiter

Responsibilities:

R&D responsible for wound drainage and suction devices

Projects:
Development of new, crystal clear drain bottles to the US market
Implement new back check valve to drain bottles
Revise specifications and drawings of supplier
Verification of new components from alternative supplier

Project Manager

Varmegye Media Kft.
Projects:

Support the tasks of web developers
Ensure the right and fluent communication between the customers and web
developers.

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