15.03.2026 aktualisiert
100 % verfügbar
Senior Automation Project Manager
Zuchwil, Schweiz
Weltweit
Bachelor of Electrical Engineering - Automation & ITSkills
21 CfrArchitekturAutomatisierungBiopharmazeutikaCanbusInformationssicherheitData IntegrationDeltavDeviceNetDigitale TechnologieDigitalisierungMessinstrumenteEthernetSCADASachgüterproduktion
SCADA/DCS/MES Architecture & Deployment
Expertise in designing and implementing complex SCADA, DCS, and MES systems for GMP-regulated biopharmaceutical and chemical manufacturing environments with proven track record in automation lifecycle ownership from concept through commissioning and validation.
Automation Project Leadership
Multi-site GMP project management experience with extensive global travel capabilities, leading automation teams and managing complex automation delivery projects across different geographical locations and regulatory environments.
Digital Transformation & Connected Plant Enablement
Strong background in GAMP 5, 21 CFR Part 11, ISA-88 & ISA-95 standards with expertise in vendor management, cross-functional collaboration between IT/OT, validation, and operations for digital manufacturing initiatives.
Control & Automation Platforms
Emerson DeltaV, Siemens S5/S7/PCS7/TIA Portal, Rockwell RSLogix/FactoryTalk, WinCC/WinCC Flexible, iFIX, B&R Automation Studio, Beckhoff TwinCAT, Schneider PL7 Pro, Mitsubishi GX, Pilz Safety PLCs
MES/Data/Digital Systems
Syncade MES, OSIsoft PI (Aveva PI), OPC-based data integration, Versiondog, TrackWise, Kneat, Veeva systems for manufacturing execution and data historization
Industrial Networks & IT/OT
Profinet, Profibus, Modbus, DeviceNet, CAN Bus, Industrial Ethernet, Virtualized server environments, basic cybersecurity and network segregation concepts
Instrumentation & Field Systems
Flow, level, pressure, temperature, conductivity, pH, humidity, particle sensors, VFDs, motors, pumps, soft starters for process control applications
GMP Compliance & Validation
FAT, SAT, IQ, OQ validation strategies ensuring compliance with GAMP 5 and 21 CFR Part 11 requirements in regulated pharmaceutical environments
Expertise in designing and implementing complex SCADA, DCS, and MES systems for GMP-regulated biopharmaceutical and chemical manufacturing environments with proven track record in automation lifecycle ownership from concept through commissioning and validation.
Automation Project Leadership
Multi-site GMP project management experience with extensive global travel capabilities, leading automation teams and managing complex automation delivery projects across different geographical locations and regulatory environments.
Digital Transformation & Connected Plant Enablement
Strong background in GAMP 5, 21 CFR Part 11, ISA-88 & ISA-95 standards with expertise in vendor management, cross-functional collaboration between IT/OT, validation, and operations for digital manufacturing initiatives.
Control & Automation Platforms
Emerson DeltaV, Siemens S5/S7/PCS7/TIA Portal, Rockwell RSLogix/FactoryTalk, WinCC/WinCC Flexible, iFIX, B&R Automation Studio, Beckhoff TwinCAT, Schneider PL7 Pro, Mitsubishi GX, Pilz Safety PLCs
MES/Data/Digital Systems
Syncade MES, OSIsoft PI (Aveva PI), OPC-based data integration, Versiondog, TrackWise, Kneat, Veeva systems for manufacturing execution and data historization
Industrial Networks & IT/OT
Profinet, Profibus, Modbus, DeviceNet, CAN Bus, Industrial Ethernet, Virtualized server environments, basic cybersecurity and network segregation concepts
Instrumentation & Field Systems
Flow, level, pressure, temperature, conductivity, pH, humidity, particle sensors, VFDs, motors, pumps, soft starters for process control applications
GMP Compliance & Validation
FAT, SAT, IQ, OQ validation strategies ensuring compliance with GAMP 5 and 21 CFR Part 11 requirements in regulated pharmaceutical environments
Erfahrung
Berufserfahrungmehr als 10 Jahre
Freelancer seit2019
Sprachen
ChinesischgutDeutschverhandlungssicherEnglischverhandlungssicherFranzösischMutterspracheSpanischGrundkenntnisse
Projekthistorie
Support remotely some of my previous clients
Led automation delivery for large-scale Drug Product and Clean Utility projects within a GMP-regulated environment. Acted as automation SME, supporting suppliers and system integrators across design, implementation, commissioning, and validation phases. Owned and reviewed automation lifecycle documentation and supported FAT, SAT, IQ, and OQ ensuring compliance with GAMP 5 and 21 CFR Part 11 requirements.
Delivered automation support for washers, autoclaves, chromatography systems, clean steam, RO/WFI systems. Created, maintained, and executed automation and validation documentation in a GxP environment. Led execution of testing protocols, deviations, and change requests, ensuring regulatory compliance.