01.11.2025 aktualisiert


100 % verfügbar
Consultant - Life sciences
Biberist, Schweiz
Weltweit
Mechanical ingenieurSkills
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
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
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
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
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
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
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
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